Anti-cancer cellular vaccine

ABSTRACT

A method for producing a cellular vaccine against any cancer is provided. The cancer cells transformed with an expression co-expressing modified interleukin-12 and a co-stimulatory molecule provides an effective means of cancer treatment since the cells can display characteristics of both cancer cells and antigen-presenting cells.

FIELD OF THE INVENTION

[0001] The present invention relates generally to the field of recombinant DNA molecules. More specifically, the present invention relates to an expression vector comprising IL-12 and a co-stimulatory molecule and methods of using same in a cancer vaccine.

BACKGROUND OF THE INVENTION

[0002] Although there is considerable evidence from scientific and clinical studies that the immune system is capable of destroying cancerous tissue, in most cases the immune system either fails to recognize the tumor or the response that is generated is too weak to be effective (Farzaneh et al., 1998, Immunol. Today 19:294). While early detection may cure tumors in many cases, once the disease becomes metastatic to distant organs, it is almost always fatal. Furthermore, the disappointing results observed with chemotherapy, radiotherapy and surgery, individually or in combination, has shifted the attention of many investigators to immunological or biological agents (Ockert et al., 1999. Immunol. Today 20:63). As such, increasing the capacity of the immune system to mediate tumor regression has been a major goal in tumor immunology. Progress towards this goal has recently been aided by the identification of immunogenic tumor antigens and by a better understanding of the mechanisms of T cell-mediated immune response and tumor escape (Boon et al., 1997, Immunol. Today 18:267; Chen, 1998, Immunol. Today 19:27).

[0003] An understanding of the mechanisms by which some animals reject tumors whereas others display progressive tumor outgrowth is gradually evolving based on an appreciation of the underlying concepts of cellular and tumor immunology. Simply put, these are that tumor cells can be eliminated by the immune system and that cellular cytotoxicity plays a major role in antitumor immunity and the effector cells in many cases are either CD8⁺ CTL or CD4⁺ Th cells (Denfeld et al., Int J. Cancer 62:259; Greten and Jaffee, 1999, J. Clin. Oncol. 17:1047; Sampson et al., 1996, Proc. Natl. Acad. Sci. USA 93:10399). However, the induction and amplification of an effective T cell-mediated immune response in malignancies characterized by poor immungenicity is the most challenging aspects of tumor vaccine development (Sampson et al., 1996). A two signal model of lymphocyte activation postulates that for optimal activation, lymphocytes require both an antigen-specific signal delivered through TCR and an antigen-nonspecific costimulatory signal (van Seventer et al., 1991 Curr. Opin. Immunol. 3:294; Linsley et al., 1991, J. Exp. Med. 173:721). In this regard, tumor cells may effectively evade the immune system by several mechanisms which are not only confined to tumor cells, but may also be related to impaired function of the immune response in a tumor bearing host (Gretten and Jaffee, 1999). These include: defective expression of MHC complex on tumor cells, antigen processing defects, lack of T cell recognition by outgrowth of antigen negative clones of tumor cells, inadequate expression of costimulatory molecules on tumor cells, inadequate expression of adhesion molecules on tumor cells, inadequate expression of Fas receptor and/or FaL expression on tumor cells, immune-suppressive cytokine secretion into tumor microenvironment, and host defense failure due to impaired immune cell function (Boon et al., 1997). Therefore, in the majority of cases the immune system either fails to recognize the tumor or the response that is generated is too weak to be effective. Furthermore, the management of residual and metastatic disease is a central problem in the treatment of tumors. During a normal immune response, full activation of antigen-specific naive T cells requires at least two distinct signals from surface receptors to proliferate in response to antigens (Young et al., 1992, J. Clin. Invest. 90:229; Allison and Krummel, 1995, Science 270:932). One of the signals is supplied by T cell receptor (TCR) engagement with peptide (antigen)-loaded major histocompatibility complex (MHC) molecules on antigen-presenting cells (APC). The second signal, at present poorly understood, can be delivered by the interaction of various molecules on the surface of T cells and the APC, one of which is the interaction of CD28 and B7-1 (Linsley et al, 1991; Young et al, 1992; Bluestone, 1995, Immunity 2:555). The combination of these two signals leads to activation, clonal expansion and differentiation into effector cells of T lymphocytes (Guerder et al., 1995, J. Immunol. 155:5167; Webb and Feldmann, 1995, Blood 86:3479; Thompson, 1995, Cell 81:979). Effector T lymphocytes, unlike naive T cells, no longer require costimulatory signals to recognize and kill antigen-bearing targets. After the immune response, a fraction of the effector cells remain as memory cells that form the basis of a faster and stronger immune response upon subsequent presentation of the same antigen (Gray, 1993, Ann. Rev. Immunol. 11:49; Ahmed and Gray, 1996, Science 272:54). The absence of second signal results in T cell clonal anergy, thus preventing clonal expansion of T lymphocytes (Chen, 1998; van Gool et al., 1994, Res. Immunol. 146:183).

[0004] Although many tumor cells express target antigens, they are generally incapable of stimulating an immune response (Boon et al., 1997; Boon and van der Bruggen, 1996, J. Exp. Med. 183:725). Cytotoxic T lymphocytes (CTL) have been recognized as a critical component of the immune response to tumors (Boon and van der Bruggen, 1996; Chen et al., 1994, J. Exp. Med. 179:523). CTL responses are sufficient to protect against tumors and can eliminate even established cancers in murine models (Mogi et al., 1998, Clin. Cancer Res. 4:713) and in humans (Gong et al., 2000, Proc. Natl. Acad. Sci. USA 97:2715). Inducing strong antigen-specific CTL responses is the goal of many current cancer vaccine strategies. The development of CTL-dependent anti-tumor immunization strategies depends on both the identification of tumor antigens recognized by CTLs and the development of methods for effective antigen delivery. CTL target tumors through recognition of a ligand consisting of a self MHC class I molecule and a peptide antigen generally derived from proteins synthesized within the tumor cell. However, for CTL induction and expansion to occur, the antigenic ligand must be presented to CTLs in the appropriate context of costimulation usually provided by professional APCs. Delivery of exogenous antigen to the endogenous MHC class I restricted processing pathway of professional APCs is a critical challenge in cancer vaccine design. Antigen delivery strategies currently under development include immunization with defined peptides, particulate proteins capable of accessing the class I pathway of professional APCs in vivo, heat shock proteins isolated from tumor cells, or adoptive transfer of antigen-loaded APCs. In addition, recent studies suggest that DNA vaccines encoding tumor antigens delivered by viral vectors or liposomes, or as naked DNA, can induce potent anti-tumor immunity.

[0005] In addition to the challenge of antigen delivery, most current tumor immunization strategies depend on the identification and production of appropriate tumor antigens. To overcome this limitation, tumor cells themselves may be used as immunogens as described in ACV (autologous cell vaccine). Engineering tumor cells to provide APC function could potentially result in polyvalent immunization to multiple tumor-specific epitopes, while obviating the need to identify specific tumor antigens. Many tumor vaccine strategies, including cytokine-transduced tumor cells, commonly referred to as gene therapy (Asher et al., 1991, J. Immunol. 146:3227; Tahara et al., 1996, Ann. NY Acad. Sci. 795:275; Lotze et al., 1996, Ann. NY Acad. Sci. 795:440; Rakhmilevich et al., 1997, Hum. Gene Ther. 8:1301; Nawrocki and Mackiewicz, 1998, Cancer Treat Rev. 25:29), synthetic peptide vaccine (Rosenberg et al., 1998, Nature Med. 4:321), tumor-antigen(peptide)-pulsed dendritic cells (Flamand et al, 1994, Eur. J. Immunol. 24:605; Bianchi et al., 1996, J. Immunol. 157:1589; Ashley et al., 1997, J. Exp. Med. 186:1177; Yang et al., 1997, Cell. Immunol. 179:84; Thurner et al., 1999, J. Exp. Med. 190:1669), and DNA vaccine (Leclerc and Ronco, 1998, Immunol. Today 19:300; Akbari et al., 1999, J. Exp. Med. 189:169) are currently under pre-clinical and clinical investigation but to date have yielded only marginal immunological and clinical response.

[0006] U.S. Pat. Nos. 5,635,188 and 5,993,829 teach a cancer vaccine comprising purified cell surface antigens shed by human cancer cell lines during culturing. The peptides are then used as a vaccine for immunization against cancer. That is, the antigens are used to sensitize the recipient's immune system to these antigens so that they are recognized in the event that tumors expressing these antigens develop.

[0007] U.S. Pat. No. 5,571,515 teaches the use of purified IL-12 protein in combination with an antigen from a pathogenic organism in a vaccine wherein IL-12 acts as an adjuvant to increase the vaccinated host's immune response to the pathogen. IL-12, either purified peptide or “naked” DNA encoding IL-12 or an expression vector containing IL-12 is administered with the vaccine either simultaneously or separately. This patent also describes a cancer vaccine, comprising a tumor antigen coadministered with purified IL-12.

[0008] U.S. Pat. No. 5,744,132 teaches methods for preparing formulations of IL-12 for use as a pharmaceutical. Specifically, the IL-12 protein is produced via an expression vector system and the IL-12 protein is recovered and lyophilized.

[0009] U.S. Pat. No. 5,891,680 teaches bioactive fusion proteins comprising, in one example, the p35 and p40 subunits of IL-12 in either order joined together by an intervening peptide linker. This patent mentions the fusion proteins as “potentially useful for the enhancement of anti-tumor immunity” but does not describe how this would be done.

[0010] U.S. Pat. No. 6,080,399 teaches a method wherein isolated antigen presenting cells are pulsed with a melanoma or similar peptide antigen. The isolated cells are then injected into patients as a vaccine in conjunction with IL-12 protein. The method teaches that subsequent injections with IL-12 are required for maximum efficiency of immune response induction.

[0011] As can be seen, these prior art patents teach the use of vaccines including IL-12 protein. However, in these instances, a finite amount of IL-12 is being supplied, and this supply diminishes over time as the protein is degraded. As a consequence, subsequent doses or injections of IL-12 may be required, as discussed above.

[0012] U.S. Pat. No. 5,922,685 describes DNA cancer vaccines which comprise p35 and p40 subunits of IL-12 under control of a single promoter (bicistronic transcript) as well as under the control of separate promoters. Furthermore, the inventors note that the non-bicistronic transcript vector (separate promoters for each subunit) was most effective. The inventors describe using the vaccine for noninvasive immunization, that is, to transfect epidermal cells and possibly mucosal surfaces.

[0013] As discussed above, methods requiring administration of peptides or proteins have inherent limitations, due to turn-over and degradation. Furthermore, the prior art does not teach methods for modifying tumor cells or cancer cells such that the cells express IL-12 and a costimulatory molecule so that the patient's immune system more effectively recognizes the tumor cell or cancer cell and elicits an immune response to destroy the tumor or cancer cells.

SUMMARY OF THE INVENTION

[0014] According to a first aspect of the invention, there is provided a method of eliciting an anti-tumor immune response in a patient comprising: isolating cancerous cells from a patient; transfecting said cancerous cells with an expression vector system comprising a DNA molecule encoding IL-12 and a costimulatory molecule operably linked to a promoter capable of directing expression of said DNA molecule in said cancerous cells; incubating said transfected cells under conditions whereby the IL-12 and the costimulatory molecules are expressed; and eliciting an anti-tumor immune response in the patient by injecting said transfected cells into the patient.

[0015] According to a second aspect of the invention, there is provided a method of vaccinating an individual comprising: providing cancerous cells isolated from a donor; transfecting said cancerous cells with an expression vector system comprising a DNA molecule encoding IL-12 and a costimulatory molecule operably linked to a promoter capable of directing expression of said DNA molecule in said cancerous cells; incubating said transfected cells under conditions whereby the IL-12 and the costimulatory molecules are expressed; isolating naive T cells from the individual; exposing the T cells to the transfected cancerous cells, thereby activating the T cells; separating the active T cells from the transfected cancerous cells; and injecting the activated T cells into the patient.

[0016] According to a third aspect of the invention, there is provided an expression system comprising a DNA molecule encoding IL-12 and a costimulatory molecule operably linked to a promoter.

[0017] According to a fourth aspect of the invention, there is provided a cancerous cell transfected with the expression system described above.

BRIEF DESCRIPTION OF THE DRAWINGS

[0018]FIG. 1 shows the overall procedure for generating DNA vector encoding IL-12 and B7-1.

[0019]FIG. 2 shows IL-12 production of IL-12 gene-transfected COS cells using ELISA.

[0020]FIG. 3 shows functional analysis of IL-12 produced by gene-transfected COS cells. Augmentation of PHA-stimulated lymphocyte proliferation was compared to standard recombinant human IL-12.

[0021]FIG. 4 shows FACS analyses of COS cell transfected with B7-1 gene. Note that unmodified or mock-transfected COS cell is negative for B7-1.

[0022]FIG. 5 shows costimulation of PHA-stimulated PBMC by B7-1 gene transfected COS cells.

[0023]FIG. 6 shows the amino acid sequence of IL12.1 (SEQ ID No. 2).

[0024]FIG. 7 shows the amino acid sequence of IL12.0 (SEQ ID No. 4).

[0025]FIG. 8 shows the amino acid sequence of IL12.3 (SEQ ID No. 6).

[0026]FIG. 9 shows the amino acid sequence of IL12.2 (SEQ ID No. 8).

[0027]FIG. 10 shows the amino acid sequence of IL12.4 (SEQ ID No. 10).

DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0028] Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which the invention belongs. Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred methods and materials are now described. All publications mentioned hereunder are incorporated herein by reference.

[0029] Definitions

[0030] As used herein, “IL-12” refers to bioactive interleukin-12. As will be appreciated by one knowledgeable in the art, this includes IL-12 assembled from p35 and p40 subunits or bioactive fragments thereof, a recombinant IL-12 comprising a fusion of p35 and p40 (or bioactive fragments thereof). The subunits may be joined by a linker.

[0031] As used herein, “costimulatory molecule” refers to molecules capable of amplifying an immune response, for example, B7-1, B7-2 and CD40L.

[0032] Described herein is a novel expression vector that comprises DNA sequences encoding IL-12 and a costimulatory molecule as well as methods of using same.

[0033] As will be appreciated by one knowledgeable in the art, any suitable control sequences (promoters, polyadenylation sites, ribosome binding sites etc) known in the art may be utilized in the expression vector.

[0034] In one embodiment, the costimulatory molecule is B7-1, although, as will be appreciated by one knowledgeable in the art, other suitable costimulatory molecules, for example, B7-2 and CD40L, may also be used.

[0035] The method of use of the vaccine comprises isolating tumor cells or cancer cells from either donors or the patient to be treated, as described below. The isolated cancer cells are transfected with the above-described expression vector and are grown under conditions such that IL-12 and the costimulatory molecule are expressed. As a result of this arrangement, the cancer cells are effectively converted to antigen presenting cells (APC). The APC cancer cells are then exposed to T cells isolated from the patient, either in vivo or ex vivo. That is, in one embodiment, the APC cancer cells are irradiated to prevent reproduction of the APC cancer cells prior to injecting the APC cancer cells into the patient. In another embodiment, T cells isolated from the patient are exposed to the APC cancer cells and are then isolated from the APC cancer cells before being injected into the patient. In both embodiments, the T cell response is activated which in turn elicits an immune response against tumors. Furthermore, once the tumor has been destroyed, memory cells remain, meaning that the patient is effectively immunized against the tumor, and a subsequent immune response will be faster and stronger.

[0036] Thus, as discussed above, the instant invention relates to the development of a new method of cancer immunotherapy and its in vitro, ex vivo, and in vivo uses. More specifically, this invention relates to the development of DNA vector comprising IL-12 and a costimulatory molecule and the protocol suitable for the in vitro generation of genetically modified human cancer cells for cancer therapy. These cells share phenotypes of both antigen presenting cells and cancer cells and are suitable as a cellular vaccine for certain types of cancer.

[0037] Since most tumor cells do not express costimulatory molecules, tumor-specific antigens are not presented to T cells efficiently (Denfeld et al., 1995; Gajewski et al., 1996, J Immunol. 156:2909). Indeed, this may represent one mechanism by which tumor cells elude recognition by the immune system. Therefore, costimulatory molecules have been expressed on the surface of tumor cells to enable them to present tumor-associated antigens, together with the costimulatory signal, directly to T cells thus obviating the need for helper T cells and APCs. In support of this model, at least in primary responses against tumors in vivo, some B7-1-expressing tumors have been found to elicit an effective response that is mediated by CD⁺ and CD⁺ T cells (Dranoff et al., 1993, Proc. Natl. Acad. Sci. USA 90:3539). In contrast, nonimmungenic tumors failed to lose tumorigenicity with the transduction of B7-1 alone (Chen et al., 1994). On the basis of these experiments, we can speculate that vaccination of tumor patients with B7 autologous tumor cells will only boost antitumor responses when the tumors are immunogenic, i.e., expresses sufficient amounts of tumor peptide-loaded MHC class-I or class-II molecules that can be recognized by the patients' T cells. An additional costimulatory signal seems to be required for inducing antitumor effector cells against poorly immunogenic tumors. In this regard, augmentation of antitumor immune responses might then be obtained by co-expressing B7 with a cytokine which up-regulate MHC molecules, attract and stimulate other immune effector cells. IL-12 has been selected for its pleiotropic effects on a variety of immune cell types and also because B7-1 and IL-12 co-operate in stimulating lymphocyte proliferation and activation in vitro (Trinchieri, 1998, Adv. Immunol. 70:83). This cytokine induces a strong local response against a number of tumors, in the context of using recombinant IL-12 paracrine secretion at the tumor site using engineered fibroblasts (Zitvogel et al., 1995, J. Immunol. 155:1393) or transformed tumor cells (Tahara et al, 1995, J. Immunol. 154:6466), as well as direct in vivo gene delivery (Rakhmilevich et al., 1997). IL-12 also elicits protective immunity against poorly immunogenic tumors and was effective in causing regression of pre-established tumors (Tahara, et al., 1995, J. Immunol. 154:6466; Cavallo et al., 1997, J. Natl. Cancer lnst. 89:1049). IL-12 stimulates the proliferation of activated T and NK cells, synergizes with IL-1 in the generation of lymphokine-activated killer cells (LAK) and enhances their lytic activity (Gately et al., 1991, J. Immunol. 147:874). Its ability to stimulate directly the production of IFN-γ both in vitro (Chan et al., 1991, J. Exp. Med. 173:869) and in vivo (Nastala et al., 1994, J. Immunol. 153:1697) and to induce primarily a Th1 response in vitro suggests its potential utility as an antitumor agent. Indeed, recent studies (Tahara et al., 1996; Brunda et al., 1996, Ann. NY Acad. Sci. 795:266) implementing systemic administration of the rIL-12 protein had profound effects on virtually every murine tumor model evaluated. Systemic administration of murine rIL-12 in several tumor models mediates profound T cell-mediated antitumor effects in vivo, leading to regression of established tumor masses, which is frequently associated with the generation of antitumor immunological memory. By the same token, however, prolonged systemic administration of rIL-12 has been related with systemic toxicity (Motzer et al., 1998, Clin. Cancer Res. 4:1183.). To address this problem, several studies on experimental tumors have evaluated the therapeutic potential of IL-12-based tumor cell vaccines and, with few exceptions, the vaccines were found to cure or significantly improve the survival of mice bearing a variety of tumors. The antitumor activity of systemic or local release of IL-12 is largely mediated by IFN-γ secreted at the tumor site by stimulated NK cells ad T cells, along with up-regulation of MHC expression on tumor cells, NOS induction, release of other cytokines, and inhibition of angiogenesis through the induction of the chemokine IP-10 by both tumor cells and infiltrating immune cells (Trinchieri, 1998).

[0038] The heterodimeric structure of IL-12 substantially complicated the construction of vectors for IL-12 production, because the expression of bioactive IL-12 requires the expression of two separate genes and subsequent correct heterodimeric assembly of the subunits (Mattner et al., 1993, Eur. J. Immunol. 23:2202). In vivo, activity of IL-12 requires the expression of the p35 and p40 subunits, which are located on different chromosomes which are regulated independently (Wolf et al., 1991, J. Immunol. 146:3074). Furthermore, it has been shown that excessive p40 subunit specifically antagonizes the effects of the IL-12 heterodimer in vitro (Mattner et al, 1993). We therefore designed a single chain recombinant IL-12 molecules by genetic recombination. Specifically, in order to achieve balanced expression of both subunits of IL-12 (p35 and p40), we generated a single chain p70 molecule by joining both subunits with various size of flexible linker. The Gly-Gly-Gly-Gly-Ser repeats were chosen for their flexibility and also because it had been used previously in constructing single chain antibodies and PIXY-321 (Curtis et al., 1991, Proc. Natl. Acad. Sci. USA 88:5809), a fused form of GM-CSF and IL-3 already in clinical use. As shown in FIG. 1, IL-12 and B7-1 were inserted into a bicistronic vector which contains an internal ribosome entry site (IRES).

[0039] In the embodiment shown in FIG. 1, the costimulatory molecule is B7-1, which enhances sensitization and activation of tumor-reactive CD⁺ T cells (Guerder et al., 1995); however, costimulatory molecules are not required for recognition and destruction of tumor cells by activated effector T cells (CTL). Moreover, it is clear that IL-12, even when present at pg/ml concentration, has profound effects on the generation of human CTLs in synergy with B7-1 stimuli (Komata et al., 1997, J. Immunother. 20:256). That is, direct activation of CTLs by tumor cells expressing B7-1 and IL-12 induces antitumor responses, bypassing the need for exogenous CD4+T cells or APCs or both, which leads to a faster and more effective antitumor response in situ. This may provide a means of eliciting effective CTL responses to tumors in patients. Thus, immunotherapy of the tumor aims to generate an effective systemic immune response capable of controlling the growth of metastatic tumors.

[0040] Our vaccine, ACV (autologous cell vaccine), utilizes cell lines derived from tumors that are modified and administered in ways that substantially enhance the response by the immune system. The cells used in the manufacture of the vaccine are sterilized by irradiation prior to administration to ensure that they are unable to replicate. The costimulatory molecule signals the immune cells in the treated patients while IL-12 recruits immune cells to the tumor site(s), and kills tumor cells by preventing angiogenesis. Our vaccine therapy would supplement existing modalities such as chemotherapy, radiotherapy and surgery by using the immune system to contain or destroy residual tumor cells, thereby increasing the length of remission, or preventing recurrence of the cancer. The immune response will be selective for the tumor and will be capable of hunting down cancer cells throughout the body.

[0041] This approach has several advantages over other above mentioned approaches that (a) it does not require the identification and purification of antigenic peptides, (b) it can be applied to almost every types of cancers, and (c) it may not induce GvHD since cancer cells are derived from self. Thus, this method will provide a new and safe therapeutic strategy for primary and metastatic cancer by activating patient's own immune system.

[0042] The present invention provides methods and compositions for use of genetically modified cancer cells to activate T cells for immunotherapeutic responses against primary or metastatic cancer. The cancer cells obtained from human donors, after transfection or transduction with the IL-12 and B7-1 expression vector described above, are administered to a cancer patient to activate the relevant T cell responses in vivo. Alternatively, T cells from patients are exposed to genetically modified cancer cells in vitro to activate the relevant T cell responses in vitro. The activated T cells are then administered to a cancer patient. In either case, the genetically modified cancer cells are advantageously used to elicit an immunotherapeutic growth-inhibiting response against a primary or metastatic tumor.

[0043] Examples of suitable vectors are discussed below and are shown in SEQ ID Nos. 1, 3, 5, 7, 9, 11, 13 and 15. As will be apparent to one knowledgeable in the art, other suitable vectors may also be used.

[0044] IL-12 fusions are shown in FIGS. 6-10 and in SEQ ID Nos. 2, 4, 6, 8, 10, 12, 14 and 16 and are discussed below.

EXAMPLE I

[0045] Construction of Vectors Encoding hB7-1 and Single Chain IL-12

[0046] Human IL-12 gene and B7-1 genes are obtained from antigen presenting cells of various tissues, for example, the spleen, bone marrow and lymph nodes as well as the circulatory system including blood and lymph. It is of note that human peripheral blood is an easily accessible ready source of antigen presenting cells and is used as a source according to a preferred embodiment of the invention. Cord blood is another source of human antigen presenting cells.

[0047] Because antigen presenting cells that express both IL-12 and B7-1 spontaneously exist in low numbers in any tissues in which they reside, including human peripheral blood, antigen presenting cells must be enriched or isolated for use. Any of a number of procedures, for example, repetitive density gradient separation, positive selection, negative selection or a combination thereof may be used to obtain enriched populations or isolated antigen presenting cells.

[0048] Once the antigen presenting cells are obtained, they are cultured in appropriate culture medium to stimulate the expression of IL-12 and B7-1. Particularly advantageous for inducing the proper state of antigen presenting cells in in vitro culture is the presence of LPS for monocytes, Anti-Ig and IL-4 or CD40 ligand (CD154) and IL-4 for B cells, or GM-CSF, IL-4 and CD40L for dendritic cells Preferred cells and conditions are of monocytes and LPS at concentration of 100-1000 ng/ml.

[0049] According to a preferred embodiment, both B7-1 and IL-12 genes have been cloned by standard recombinant DNA techniques. The cDNA encoding the p35 and p40 chains of human IL-12 and human B7-1 were generated from LPS-stimulated human peripheral blood monocytes by reverse transcriptase-PCR.

[0050] Primers selected from the 5′ and 3′-end of the coding sequences of each gene were designed to introduces the appropriate restriction sites for further genetic recombinations, as shown in FIG. 1.

[0051] After cloning of B7.1 and IL-12, each gene was subcloned into a vector.

[0052] Specifically, B7-1 was excised at appropriate restriction sites and inserted into MCS A site on pIRES excised with corresponding restriction digests or into MCS B site excised with corresponding restriction enzyme generating pIRES-hB7-1 (A) and pIRES-hB7-1(B).

[0053] The cDNA for the single chain IL-12 fusion protein was constructed by linkage of the p40 and p35 cDNAs with a synthetic flexible linker. We have utilized three different linkers that have 2, 3 and 4 repeats of Gly-Gly-Gly-Gly-Ser (shown in FIGS. 9, 8 and 10, respectively). These products (about 1.6 kb) have been cloned into pGEM-T easy vector generating pGEM-IL12.2, pGEM-IL12.3, and pGEM-IL12.4. PCR products from these three vectors were digested with appropriate sets of restriction enzyme and ligated into the MCS B on pIRES-hB7-1 (A) or into the MCS A on pIRES-hB7-1(B) generating 2 series (pIRES-hB7-1-IL12 and pIRES-IL12-hB7-1 series) of 6 different expression vectors (pIRES-hB7-1-IL12.2 (SEQ ID No. 7), pIRES-hB7-1-IL12.3 (SEQ ID No. 5), and pIRES-hB7-1-IL12.4 (SEQ ID No. 9); pIRES-IL12.2-hB7-1 (SEQ ID No. 15), pIRES-IL12.3-hB7-1 (SEQ ID No. 13), and pIRES-IL12.4-hB7-1 (SEQ ID No. 11)). In addition, constructs with a single linker (IL12.1, shown in FIG. 6; SEQ ID No. 2) and no linker (IL12.0, shown in FIG. 7; SEQ ID No. 4) were used to construct pIRES-hB7.1-IL12.1 (SEQ ID No. 1) and pIRES-hB7.1-IL12.0 (SEQ ID No. 3) respectively. Constructs were sequenced across all cloning junctions to determine the fidelity of recombination process.

EXAMPLE II

[0054] Gene Transfer into Cancer Cells

[0055] According to the present invention, the pIRES DNA vectors are introduced into a desired cancer cells by lipofectamin. After gene transfection, cells are analyzed to assess the expression of both IL-12 by ELISA and B7-1 by FACS.

[0056] Alternatively, DNA vectors can be introduced into cancer cells by other means known in the art, for example, PEG, electroporation, DEAE-dextran method or calcium phosphate method.

[0057] After 24-72 hr culture, supernatants were collected for IL-12 ELISA and bioassay and cells were collected for B7-1 expression and costimulation assay.

EXAMPLE III

[0058] Applications or Methods of use of Genetically Modified Cancer Cell's to Stimulate T Cells Against Cancer in vitro and in vivo

[0059] According to a preferred embodiment of the invention, cancer tissues are obtained from a patient to be treated to generate a cancer cell line. The cell lines are in turn used to activate autologous T cells of the patient, either in vitro or in vivo, for cancer immunotherapy and/or tumor growth inhibition.

[0060] According to another embodiment, a tumor cell recovered from surgical specimens without further treatment can be used for gene transfer, as discussed herein.

[0061] Using an approach wherein the patient's own cancer cells that are genetically modified provides the following advantages: (A) identification of cancer antigen is not required; (B) temporal expression of genes eliminates dangerous side effects; (C) antigen on cancer cells along with costimulatory factor, B7-1, is presented to T lymphocytes; (D) the use of B7-1 on and IL-12 from cancer cell surface eliminates the need to provide T cells with IL-2 or other cytokines either in the form of the cytokine itself or transfection of the cDNA into specific cells; (E) all procedures are carried out using the patient's own cells.

EXAMPLE IV

[0062] Cell Lines and Reagents

[0063] Cell lines are established from pathologically proven cancer tissues. Soild tumors were first finely minced with scissors and dissociated into small aggregates by pipetting. Appropriate amounts of fine neoplastic-tissue fragments were seeded into 25 cm² flasks. Tumor cells were initial cultured in RPMI-1640 medium containing 10% heat-inactivated fetal calf serum. After establishment, passages were performed when heavy tumor cell growth is observed. If stromal cell growth is noted in initial cultures, differential trypsinization is used to obtain a pure tumor cell population. Established human cancer cells are maintained in culture in RPMI 1640. Mouse monoclonal anti-human CD80 and isotype-matched control antibodies were purchased from Becton-Dickinson, San Jose, Calif.

EXAMPLE V

[0064] Cancer Patients

[0065] Patients with a histologic confirmation of cancer are selected for this study which included a signed informed consent. 50 ml of heparinized peripheral blood were drawn every 2 weeks during the period of observation which continues. Details regarding clinical stage, hematologic status, and other relevant treatments are recorded.

EXAMPLE VI

[0066] Isolation of Monocytes and Stimulation With LPS

[0067] Peripheral blood was drawn from normal donors and was subjected to Ficoll-Hypaque (Pharmacia, Uppssala, Sweden) density gradient centrifugation. After washing twice with Hank's Balanced salt solution (HBSS, Life Technologies, Grand Island, N.Y.), monocytes were separated according to their plastic adherence (Steinbach et al., 1998, Res. Immunol. 149:627; Thurner et al., 1999, J. Immunol. Methods 223:1) for 30 min -1 hr incubation in 5% CO₂, 37° C. incubator. Enriched monocytes were cultured in the presence of 100-1000 ng/ml of LPS (Sigma Chem. Co., St. Louis, Mo.). Alternatively, monocytes are purified from eripheral blood mononuclear cells by positive selection by CD14-MACS column (Miltenyi Biotec). After 16-24 hr of incubation, cells were treated with Trizol (Life Technologies) for RNA preparation and subsequent gene cloning.

EXAMPLE VII

[0068] Construction of Vectors Encoding HB7-1 and Single Chain IL-12

[0069] Both B7-1 and IL-12 genes were cloned by standard recombinant DNA techniques, as discussed herein. The cDNA encoding the p35 and p40 chains of human IL-12 and human B7-1 were generated from 1 μg/ml of LPS-stimulated human peripheral blood monocytes or CD40 ligand and IL4 stimulated human B cells by reverse transcriptase- PCR. Typically, peripheral blood monocytes were utilized for experimental convenience. First, mRNA was isolated by oligo-dT MACS column (Miltenyi Biotec) and subjected to first strand cDNA synthesis. Primers selected from the 5′ and 3′-end of the coding sequences of each gene were designed to introduces restriction sites. PCR was done with PCR-premix (Bioneer, Cheongwon, Chungbuk, Korea) containing PCR buffer, dNTP, Taq polymerase and MgCl₂. After cloning of B7.1, each gene has been subcloned into PGEM vector generating pGEM-hp40, pGEM-hp35, and pGEM-hB7-1 and clones were verified by sequencing.

[0070] Next, the PCR product of hB7-1 was either excised at appropriate restriction sites and inserted into MCS A site on pIRES or into MCS B site excised with restriction enzymes generating pIRES-hB7-1 (A) and pIRES-hB7-1(B).

[0071] The CDNA for the single chain IL-12 fusion protein was constructed by linkage of the p40 and p35 cDNAs with synthetic linkers of 2, 3 and 4 repeats of Gly-Gly-Gly-Gly-Ser containing NcoI restriction sites. The p40 from pGEM-hp40 has been amplified with linker-containing primers producing p40L2, p40L3, and p40L4. The p35 was cloned downstream of the linker with restriction site. These products (about 1.6 kb) have been cloned into pGEM-T easy vector generating pGEM-IL12.2, pGEM-IL12.3, and pGEM-IL12.4. PCR products from these three vectors were digested with the appropriate restriction enzymes and ligated into the MCS B on pIRES-hB7-1 (A) or into restriction site of MCS A on pIRES-hB7-1(B) generating 2 series (pIRES-hB7-1-IL12 and pIRES-IL12-hB7-1 series) of 6 different expression vectors (pIRES-hB7-1-IL12.2, pIRES-hB7-1-IL12.3, and pIRES-hB7-1-IL12.4; pIRES-IL12.2-hB7-1, pIRES-IL12.3-hB7-1, and pIRES-IL12.4-hB7-1). Constructs were sequenced across all cloning junctions to determine the fidelity of recombination process.

EXAMPLE VII

[0072] Transfection of Plasmid Encoding IL-12/B7-1 Genes and Analysis of Gene Expression

[0073] COS-7 cells or human cancer cell lines in 6-well plates at 60-70% confluency were transfected with 5 μg of vector prepared by Qiagen plasmid kit (Qiagen Inc, Valencia, Calif.) using Lipofectin (Life Technologies) according to manufacturer's instructions. After 5 hr incubation at 37° C., the DNA/Lipofectin mixture was removed and replaced with fresh medium. After 48 hr, supernatants were collected for IL-12 ELISA and bioassay, and cells were collected for B7-1 expression. IL-12 in the culture supernatants of transfected cells was quantitated using human IL-12 p70 ELISA kit (Endogen, Woburn, Mass.). The function of IL-12 produced by gene transfected cells can be analyzed by PHA-blast assay (Gately et al., 1991) and/or IFN-γ induction assay of PHA-stimulated PBMC. B7-1 expression on gene-transfected cells can be analyzed by flow cytometer after staining with monoclonal anti-B7-1 antibody, while the function of B7-1 can be analyzed by proliferation of PBMC stimulated with sub-optimal dose of PHA in the presence of gene-transfected cells.

EXAMPLE IX

[0074] Collection of Tissue and Preparation Cells

[0075] Patients with a histologic confirmation of cancer were selected for this study which included a signed informed consent. 50 ml of heparinized peripheral blood was drawn. Details regarding clinical stage, hematologic status, and other relevant treatments were recorded. Cancer cell lines were established from patients. Solid tumors were finely minced with scissors and dissociated into small aggregates by pipetting. Appropriate amounts of fine tissue fragments were seeded into 25 cm² flasks. In most cases, tumor cells were cultured in RPMI-1640 medium supplemented with 10% heat inactivated FCS. Initial passages were performed when heavy tumor cell growth was observed; subsequent passages were performed once or twice a week. Adherent cell cultures were passaged at sub-confluency after trypsin-EDTA (Life Technologies) treatment, and floating cells were passaged after dissociation, if necessary, of the cells by pipetting. If stromal cell or fibroblast growth was noted in initial cultures, differential trypsinization was used to obtain a pure tumor cell population. All cultures were maintained in humidified incubators at 37° C. in an atmosphere of 5% CO₂ and 95% air. Phenotypes of established cell lines were analyzed with FACS (Becton Dickinson) after fluorochrome-labeled monoclonal antibody staining.

EXAMPLE X

[0076] Construction of DNA Vectors Encoding hB7-1 and Single Chain IL-12

[0077] Mononuclear cells were isolated by Ficoll-Paque (Pharmacia) density gradient centrifugation of heparinized blood obtained from healthy adult donors according to standard protocols. Then, cells (5×10⁶/ml, 10 ml) resuspended in RPMI-1640 medium supplemented with 10% FCS, 10 mM of glutamine, and penicillin/streptomycin and subjected to 1 hr plastic adherence. Non-adherent mononuclear cells were removed by rinsing with warm PBS and remaining monocytes were stimulated with LPS(1 μg/ml, Sigma) for 20 hr at 37° C., 5% CO₂ incubator. Both B7-1 and IL-12 genes have been cloned by standard recombinant DNA techniques. The cDNA encoding the p35 and p40 chains of human IL-12 and human B7-1 were generated from LPS-stimulated human peripheral blood monocytes by reverse transcriptase-PCR. Primers selected from the 5′ and 3′-end of the coding sequences of each gene were designed to introduces SalI, NcoI, NotI, NheI and MluI restriction sites. After cloning of B7.1, each gene has been subcloned into pGEM vector generating pGEM-hp40, pGEM-hp35, and pGEM-hB7-1 and clones were verified by sequencing.

[0078] The sets of 5′ and 3′ primers for PCR were hp4F 5′-CTAGCTAGCGGCCCAGAG CMGATGTG-3′, hp4° F.b 5′-ACGCGTCGACGGCCCGAGCMGATGTG-3′, and hp40R1 5′-ACTGCAGGGCACAGATGC-3′ for p40, hp35F 5′-CATGCCATGGAG M ACCTCCCCGTGGC-3′, hp35R 5′-CCGACGCGTACCTCGCTTTTTAGGAAGCAT-3′, and hp35Rb 5′-ATMGAATGCGGCCGCACCTCGCTTTTTAGGAAGCAT-3′ for p35, and hB7-1 F 5′-ACGAGTCGACATGGGCCACACACGGA-3′, hB7-1 R 5′-GGCGGCC GTTTCAGCCCCTTGCTTTT-3′, hB7. 1 Fb 5′-CTAGCTAGCATGGGCCACACACGG A-3′, and hB7.1 Rb 5′-CCGACGCGTTTTCAGCCCCTTGCTTCT-3′ for B7.1

[0079] Next, PCR product of hB7-1 has been either excised at NheI/MluI or at Sall/Notl and inserted into MCS A site on pIRES excised with NheI/MluI or into MCS B site excised with SalI/NotI generating pIRES-hB7-1 (A) and pIRES-hB7-1(B).

[0080] The cDNA for the single chain IL-12 fusion protein was constructed by linkage of the p40 and p35 cDNAs with a synthetic linker containing Ncol restriction sites. Previous studies suggested that an accessible N-terminus of the p40 subunit is important for IL-12 bioactivity. When the p35 subunit came before the p40 subunit, there was greatly decreased IL-12 activity, in contrast, when the subunits were reversed, with p40 in front of p35, the single chain IL-12 had biological activity comparable to rIL-12.

[0081] We have utilized three different linkers that have 2, 3 and 4 repeats of Gly-Gly-Gly-Gly-Ser. The p40 from pGEM-hp40 has been amplified with linker-containing primers producing p40L2, p40L3, and p40L4. The p35 was cloned down stream of the linker with Ncol restriction site. These products (about 1.6 kb) have been cloned into pGEM-T easy vector generating pGEM-IL12.2, pGEM-IL12.3, and pGEM-IL12.4. PCR products from these three vectors were digested with SalI/NotI or NheI/MluI and ligated into the MCS B on pIRES-hB7-1(A) or into NheI/MluI site of MCS A on pIRES-hB7-1(B) generating 2 series (pIRES-hB7-1-IL12 and pIRES-IL12-hB7-1 series series) of 6 different expression vectors (pIRES-hB7-1-IL12.2, pIRES-hB7-1-IL12.3, and pIRES-hB7-1-IL12.4; pIRES-IL12.2-hB7-1, pIRES-IL12.3-hB7-1, and pIRES-IL12.4-hB7-1). Constructs were sequenced across all cloning junctions to determine the fidelity of recombination process.

[0082] In some cases, peripheral blood monocytes were subjected to MACS purification to further enrich monocyte fraction. Cells stained with CD14-microbeads (Milteyi Biotec) in the presence of FcR blocking reagent (human IgG) for 30 minutes at 4° C. After washing cells applied to MS+ column which was subjected to magnetic fields. Cells remaining in the column were collected and washed once before undergoing culturing as indicated above.

EXAMPLE XI

[0083] IL-12 Production by Gene-Modified COS Cells

[0084] IL-12 in the culture supernatants of transfected cells was quantitated using human IL-12 p70 ELISA kit (Endogen). After transfection, culture supernatants of COS cells were harvested, filtered with 0.22 μm syringe filter, and stored until analyzing the quantity and quality of gene expression.

[0085] While cells transfected with pIRES-hB7-1-IL12 series(pIRES-hB7-1-IL12.2, pIRES-hB7-1-IL12.3, and pIRES-hB7-1-IL12.4) produced 0.6-1.5 ng/ml, culture supernatants from cells with pIRES-IL12-hB7-1 series (pIRES-IL12.2-hB7-1, pIRES-IL12.3-hB7-1, and pIRES-IL12.4-hB7-1) contained 21-32 ng/ml of IL-12 according to ELISA analysis.

[0086] All three vectors with different length of flexible linkers produced similar quantities of IL-12 indicating that the linker length did not influence the level of gene expression or conformation of IL-12.

EXAMPLE XII

[0087] Bioactivity Measurement of IL-12 Produced by Transfected COS Cells

[0088] Assays for IL-12 induced proliferation of PBMC were performed as previously described (Gately et al., 1991, J. Immunol. 147:874.). PBMC were isolated from normal blood donors by Ficoll-Hypaque density centrifugation (Pharmacia, Piscataway, N.J.). These cells were then depleted of monocytes by plastic adherence, and non adherent cells were resuspended at 5×10⁵ cells/ml in RPMI-1640 supplemented with 10% FCS, penicillin, streptomycin, L-glutamine containing 2 μg/ml of PHA(Sigma) and were cultured for 3 days. Cells were then washed and recultured with rIL-2 (20 iu/ml) for an additional 48 hr. The PHA-blasts were then washed with acidified RPMI-1640 (pH 6.4) and rest for 4 hr in RPMI-1640 supplemented with 0.5% human AB serum. The cell concentration was adjusted to 2×10⁶ cells/ml in complete medium. 50 μl of serial 1:5 dilutions of IL-12 standard (Leinco Tech) and culture supernatants of transfected cells were made in complete medium over a range of 0.16 pg to 200 pg/mi. Next, 50 μl cell suspension (PHA-blasts) was mixed with these serial diutions in triplicate in a flat-bottomed 96-well tissue culture plate. Neutralizing anti-IL-2 antibody was included to block IL-2-induced proliferation. [³H]-Thymidine (1 μCi/well, NEN, Boston, Mass.) was added to the wells after 36 hr of culture at 37 C, 5%CO₂. After an additional 16 hr of incubation, cultures were harvested onto glass filters, and radioactivity was assessed by liquid scintillation.

[0089] The bioactivity of IL-12 produced by vector-transfected cell lines was also measured using an assay based on the ability of this cytokine to stimulate production of IFN-γ by lymphocytes. PBMC activated with PHA 5 ug/ml for 5 days were collected, washed and restimulated with serial dilutions of standard IL-12 (1-1000 pg/ml) and culture supernatants from transfected cell lines stimulated. Following a 20 hr incubation, culture supernatants of PBMC were harvested and assayed for IFN-γ by ELISA (Endogen). The assay for IL-12 was quantified by comparing the amount of IFN-γ produced in the test samples with that induced by the recombinant IL-12 standards.

[0090] In accordance with ELISA data, the bioactivity of IL-12 in the culture supernatants of pIRES-hB7-1-IL12 series was significantly lower than that of pIRES-IL12-hB7-1 series. In PHA-blast assays, IL-12 produced by transfected COS cells efficiently induced the proliferation of T cells and NK cells comparable to the standard IL-12. Moreover, in IFN-γ induction assay, the specific activity of IL-12 produced by vector transfected cells at equal concentration was almost identical or even better to rIL-12 standard.

EXAMPLE XII

[0091] B7-1 Expression on Gene-Modified Cells by Flow Cytometric Analysis

[0092] Assessment of B7-1 on vector transfected COS-7 was done with the aid of FITC-conjugated anti-B7-1 (Pharmingen, San Diego, Calif.). As a control, we used an appropriate FITC-conjugated isotype-matched normal IgG1 (Pharmingen). Flow cytometric analysis of 10,000 viable cells was conducted on a FACS vantage (Becton Dickinson). Each experiments was repeated at least three times, and the results of a representative experiment are provided in the form of a histogram.

[0093] While a significant proportion (20-30%) of cells transfected with pIRES-B7-1-IL12 series expressed B7-1, little (less than 5%) was shown on cells transfected with pIRES-IL12-hB7-1 series.

EXAMPLE XIII

[0094] B7-1-induced Costimulation

[0095] T lymphocytes were purified with T cell enrichment kit (Miltenyi Biotech). Allogneic T lymphocytes (1×10⁶ cells/ml) were co-cultured with irradiated (3000 rad) vector-transfected ME-180 (1, 2, 4, 8×10⁴ cells/ml) in 96 well flat-bottomed plates in the presence of 1 ug/ml of PHA. In some cases, murine CD28-Fc (Chemicon) was included to determine the direct effects of B7-1 expressed on vector-transfected ME-180. 48 hr later, each well received 1 μCi [³H]-thymidine, and after an additional 16 hr, cultures were harvested onto glass filters, and radioactivity was assessed by liquid scintillation.

[0096] While a significant T cell costimulatory activity (50-100 fold higher cpm over background) was shown by cells transfected with pIRES-B7-1-IL12 series, only a minor (3 fold higher cpm over background) was detected on cells transfected with pIRES-IL12-hB7-1 series. Furthermore, there was a dose-dependent inhibition of costimulatory activity by chimeric CD28-Fc protein, suggesting the major costimulation was provided directly by B7-1 on vector-transfected ME-180.

EXAMPLE XIV

[0097] Cytotoxicity Assay

[0098] PBMC (1×10⁷ cells) from normal donors were stimulated with ME-180 in a volume of 10 ml. After 6 days, effector cells were collected, adjusted to 2×10⁶ cells/ml, and titrated in triplicate in flat-bottomed plates to give the indicated E:T ratios along with vector-transfected ME-180 cells. Supernatants were collected after 4 hr and cytotoxicity was measured by the kit purchased from Roche (Manheim, Germany). Percentage-specific lysis was calculated according to the manufacturer's instructions.

[0099] While a significant cytotoxicity was shown by PBMC co-cultured with ME-180 cells transfected with pIRES-B7-1, only a minor cytotoxicity was detected on PBMC co-cultured with ME-180. The co-toxic effects of PBMC co-cultured with ME-180 cells transfected with pIRES-B7-1 were exerted not only to pIRES-B7-1-IL12 series and pIRES-IL12-B7-1 series but also to unmodified ME-180, suggesting the maturation of effector CTL by B7-¹⁺ ME-180 during co-culture and implicating the immunotherapeutic potential of ACV.

[0100] Once generated, IL-12 and B7-1 genetically-modified cancer cells can, if desired, be injected by any standard method into the patient. Preferably, the cells are injected back into the same patient from whom the source cancer cells were obtained. The injection site may be subcutaneous, intraperitoneal, intramuscular, intradermal, or intravenous. The number of cells injected into the patient in need of treatment is according to standard protocols, e.g., 1×10⁴ to 1×10⁶ are injected back into the individual. The number of cells used for treating any of the disorders described herein varies depending upon the manner of administration, the age and the body weight of the subject, and the condition of the subject to be treated, and ultimately will be decided by the attending physician.

[0101] The methods and media compositions described herein are useful for the culture and production of cancer cells and gene-modified cancer cells in vitro and in vivo. Given the capacity of gene-modified cancer cells to elicit strong antigen-specific helper and cytotoxic T cell responses, the ability to generate large numbers of homogeneous preparations of cancer cells facilitates the manipulation of these cells for the development of a variety of therapies, including without limitation, ex vivo and in vivo human therapies.

[0102] The invention therefore encompasses the use of gene-modified cells produced according to the methods of the invention for any number of human or veterinary therapeutics. For example, vector types other than above mentioned combination of genes can be produced as described herein can be used in ex vivo cell transplantation therapies for the treatment of a variety of human diseases, e.g., disorders of the immune system. Accordingly, such cells are useful for modulating autoimmunity and limiting a variety of autoimmune diseases.

[0103] Gene-modified cancer cells also find use in the ex vivo expansion of T cells, e.g., CD4⁺ cells or CD8⁺ cells or both. Thus, such cells are useful for stimulating the proliferation and reconstitution of CD4⁺ cells or CD8⁺ cells or both in a human having an immune disorder. Reconstitution of the immune system, e.g., a patient's CD4⁺ cells, is useful in immunotherapy for preventing, suppressing, or inhibiting a broad range of immunological disorders, e.g., as found during HIV infection.

[0104] The cancer cells described herein are also useful for vaccine development. For example, administration of antigens (as a form of cell lysate) to immuno-competent host further facilitate the use of these cells for active immunization in situ.

[0105] In addition, gene-modified cancer cells are useful for the generation of antibodies (e.g., monoclonal antibodies) that recognize cancer cell-specific markers. Anti-cancer cell antibodies are produced according to standard hybridoma technology. Such antibodies are useful for the evaluation and diagnosis of a variety of immunological disorders.

[0106] In some embodiments, the ACV as described herein at therapeutically effective concentrations or dosages may be combined with a pharmaceutically or pharmacologically acceptable carrier, excipient or diluent, either biodegradable or non-biodegradable. Exemplary examples of carriers include, but are by no means limited to, for example, poly(ethylene-vinyl acetate), copolymers of lactic acid and glycolic acid, poly(lactic acid), gelatin, collagen matrices, polysaccharides, poly(D,L lactide), poly(malic acid), poly(caprolactone), celluloses, albumin, starch, casein, dextran, polyesters, ethanol, mathacrylate, polyurethane, polyethylene, vinyl polymers, glycols, mixtures thereof and the like. Standard excipients include gelatin, casein, lecithin, gum acacia, cholesterol, tragacanth, stearic acid, benzalkonium chloride, calcium stearate, glyceryl monostearate, cetostearyl alcohol, cetomacrogol emulsifying wax, sorbitan esters, polyoxyethylene alkyl ethers, polyoxyethylene castor oil derivatives, polyoxyethylene sorbitan fatty acid esters, polyethylene glycols, polyoxyethylene stearates, colloidol silicon dioxide, phosphates, sodium dodecylsulfate, carboxymethylcellulose calcium, carboxymethylcellulose sodium, methylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, hydroxypropylmethycellulose phthalate, noncrystalline cellulose, magnesium aluminum silicate, triethanolamine, polyvinyl alcohol, polyvinylpyrrolidone, sugars and starches. See, for example, Remington: The Science and Practice of Pharmacy, 2000, Gennaro, AR ed., Eaton, Pa.: Mack Publishing Co.

[0107] The invention provides kits for carrying out the methods of the invention. Accordingly, a variety of kits are provided. The kits may be used for any one or more of the following (and, accordingly, may contain instructions for any one or more of the following uses): treating some forms of cancer in an individual; preventing the spread or metastasis of some forms of cancer; preventing one or more symptoms of some forms of cancer; reducing severity of one or more symptoms associated with cancer; delaying development of cancer in an individual; or vaccinating an individual against some forms of cancer.

[0108] The kits of the invention comprise one or more containers comprising the ACV and a suitable excipient as described herein and a set of instructions, generally written instructions although electronic storage media (e.g., magnetic diskette or optical disk) containing instructions are also acceptable, relating to the use and dosage of the ACV for the intended treatment. The instructions included with the kit generally include information as to dosage, dosing schedule, and route of administration for the intended treatment. The containers of the ACV may be unit doses, bulk packages (e.g., multi-dose packages) or sub-unit doses.

[0109] The ACV may be packaged in any convenient, appropriate packaging.

[0110] As will be appreciated by one knowledgeable in the art, the anti-cancer vaccine may be combined or used in combination with other treatments known in the art.

[0111] While the preferred embodiments of the invention have been described above, it will be recognized and understood that various modifications may be made therein, and the appended claims are intended to cover all such modifications which may fall within the spirit and scope of the invention.

1 16 1 8578 DNA Artificial Sequence enhancer (1)..(659) CMV IE 1 tcaatattgg ccattagcca tattattcat tggttatata gcataaatca atattggcta 60 ttggccattg catacgttgt atctatatca taatatgtac atttatattg gctcatgtcc 120 aatatgaccg ccatgttggc attgattatt gactagttat taatagtaat caattacggg 180 gtcattagtt catagcccat atatggagtt ccgcgttaca taacttacgg taaatggccc 240 gcctggctga ccgcccaacg acccccgccc attgacgtca ataatgacgt atgttcccat 300 agtaacgcca atagggactt tccattgacg tcaatgggtg gagtatttac ggtaaactgc 360 ccacttggca gtacatcaag tgtatcatat gccaagtccg ccccctattg acgtcaatga 420 cggtaaatgg cccgcctggc attatgccca gtacatgacc ttacgggact ttcctacttg 480 gcagtacatc tacgtattag tcatcgctat taccatggtg atgcggtttt ggcagtacac 540 caatgggcgt ggatagcggt ttgactcacg gggatttcca agtctccacc ccattgacgt 600 caatgggagt ttgttttggc accaaaatca acgggacttt ccaaaatgtc gtaacaactg 660 cgatcgcccg ccccgttgac gcaaatgggc ggtaggcgtg tacggtggga ggtctatata 720 agcagagctc gtttagtgaa ccgtcagatc actagaagct ttattgcggt agtttatcac 780 agttaaattg ctaacgcagt cagtgcttct gacacaacag tctcgaactt aagctgcagt 840 gactctctta aggtagcctt gcagaagttg gtcgtgaggc actgggcagg taagtatcaa 900 ggttacaaga caggtttaag gagaccaata gaaactgggc ttgtcgagac agagaagact 960 cttgcgtttc tgataggcac ctattggtct tactgacatc cactttgcct ttctctccac 1020 aggtgtccac tcccagttca attacagctc ttaaggctag agtacttaat acgactcact 1080 ataggctaga tgggccacac acggaggcag ggaacatcac catccaagtg tccatacctc 1140 aatttctttc agctcttggt gctggctggt ctttctcact tctgttcagg tgttatccac 1200 gtgaccaagg aagtgaaaga agtggcaacg ctgtcctgtg gtcacaatgt ttctgttgaa 1260 gagctggcac aaactcgcat ctactggcaa aaggagaaga aaatggtgct gactatgatg 1320 tctggggaca tgaatatatg gcccgagtac aagaaccgga ccatctttga tatcactaat 1380 aacctctcca ttgtgatcct ggctctgcgc ccatctgacg agggcacata cgagtgtgtt 1440 gttctgaagt atgaaaaaga cgctttcaag cgggaacacc tggctgaagt gacgttatca 1500 gtcaaagctg acttccctac acctagtata tctgactttg aaattccaac ttctaatatt 1560 agaaggataa tttgctcaac ctctggaggt tttccagagc ctcacctctc ctggttggaa 1620 aatggagaag aattaaatgc catcaacaca acagtttccc aagatcctga aactgagctc 1680 tatgctgtta gcagcaaact ggatttcaat atgacaacca accacagctt catgtgtctc 1740 atcaagtatg gacatttaag agtgaatcag accttcaact ggaatacaac caagcaagag 1800 cattttcctg ataacctgct cccatcctgg gccattacct taatctcagt aaatggaatt 1860 tttgtgatat gctgcctgac ctactgcttt gccccaagat gcagagagag aaggaggaat 1920 gagagattga gaagggaaag tgtacgccct gtataacagt gtccgcagaa gcaaggggct 1980 gaaaacgcgt cgagcatgca tctagggcgg ccaattccgc ccctctccct cccccccccc 2040 taacgttact ggccgaagcc gcttggaata aggccggtgt gcgtttgtct atatgtgatt 2100 ttccaccata ttgccgtctt ttggcaatgt gagggcccgg aaacctggcc ctgtcttctt 2160 gacgagcatt cctaggggtc tttcccctct cgccaaagga atgcaaggtc tgttgaatgt 2220 cgtgaaggaa gcagttcctc tggaagcttc ttgaagacaa acaacgtctg tagcgaccct 2280 ttgcaggcag cggaaccccc cacctggcga caggtgcctc tgcggccaaa agccacgtgt 2340 ataagataca cctgcaaagg cggcacaacc ccagtgccac gttgtgagtt ggatagttgt 2400 ggaaagagtc aaatggctct cctcaagcgt attcaacaag gggctgaagg atgcccagaa 2460 ggtaccccat tgtatgggat ctgatctggg gcctcggtgc acatgcttta catgtgttta 2520 gtcgaggtta aaaaaacgtc taggcccccc gaaccacggg gacgtggttt tcctttgaaa 2580 aacacgatga taagcttgcc acaacccggg atcctctaga gtcgacggcc cagagcaag 2639 atg tgt cac cag cag ttg gtc atc tct tgg ttt tcc ctg gtt ttt ctg 2687 Met Cys His Gln Gln Leu Val Ile Ser Trp Phe Ser Leu Val Phe Leu 1 5 10 15 gca tct ccc ctc gtg gcc ata tgg gaa ctg aag aaa gat gtt tat gtc 2735 Ala Ser Pro Leu Val Ala Ile Trp Glu Leu Lys Lys Asp Val Tyr Val 20 25 30 gta gaa ttg gat tgg tat ccg gat gcc cct gga gaa atg gtg gtc ctc 2783 Val Glu Leu Asp Trp Tyr Pro Asp Ala Pro Gly Glu Met Val Val Leu 35 40 45 acc tgt gac acc cct gaa gaa gat ggt atc acc tgg acc ttg gac cag 2831 Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile Thr Trp Thr Leu Asp Gln 50 55 60 agc agt gag gtc tta ggc tct ggc aaa acc ctg acc atc caa gtc aaa 2879 Ser Ser Glu Val Leu Gly Ser Gly Lys Thr Leu Thr Ile Gln Val Lys 65 70 75 80 gag ttt gga gat gct ggc cag tac acc tgt cac aaa gga ggc gag gtt 2927 Glu Phe Gly Asp Ala Gly Gln Tyr Thr Cys His Lys Gly Gly Glu Val 85 90 95 cta agc cat tcg ctc ctg ctg ctt cac aaa aag gaa gat gga att tgg 2975 Leu Ser His Ser Leu Leu Leu Leu His Lys Lys Glu Asp Gly Ile Trp 100 105 110 tcc act gat att tta aag gac cag aaa gaa ccc aaa aat aag acc ttt 3023 Ser Thr Asp Ile Leu Lys Asp Gln Lys Glu Pro Lys Asn Lys Thr Phe 115 120 125 cta aga tgc gag gcc aag aat tat tct gga cgt ttc acc tgc tgg tgg 3071 Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly Arg Phe Thr Cys Trp Trp 130 135 140 ctg acg aca atc agt act gat ttg aca ttc agt gtc aaa agc agc aga 3119 Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe Ser Val Lys Ser Ser Arg 145 150 155 160 ggc tct tct gac ccc caa ggg gtg acg tgc gga gct gct aca ctc tct 3167 Gly Ser Ser Asp Pro Gln Gly Val Thr Cys Gly Ala Ala Thr Leu Ser 165 170 175 gca gag aga gtc aga ggg gac aac aag gag tat gag tac tca gtg gag 3215 Ala Glu Arg Val Arg Gly Asp Asn Lys Glu Tyr Glu Tyr Ser Val Glu 180 185 190 tgc cag gag gac agt gcc tgc cca gct gct gag gag agt ctg ccc att 3263 Cys Gln Glu Asp Ser Ala Cys Pro Ala Ala Glu Glu Ser Leu Pro Ile 195 200 205 gag gtc atg gtg gat gcc gtt cac aag ctc aag tat gaa aac tac acc 3311 Glu Val Met Val Asp Ala Val His Lys Leu Lys Tyr Glu Asn Tyr Thr 210 215 220 agc agc ttc ttc atc agg gac atc atc aaa cct gac cca ccc aac aac 3359 Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys Pro Asp Pro Pro Asn Asn 225 230 235 240 ttg cag ctg aag cca tta aag aat tct cgg cag gtg gag gtc agc tgg 3407 Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg Gln Val Glu Val Ser Trp 245 250 255 gag tac cct gac acc tgg agt act cca cat tcc tac ttc tcc ctg aca 3455 Glu Tyr Pro Asp Thr Trp Ser Thr Pro His Ser Tyr Phe Ser Leu Thr 260 265 270 ttc tgc gtt cag gtc cag ggc aag agc aag aga gaa aag aaa gat aga 3503 Phe Cys Val Gln Val Gln Gly Lys Ser Lys Arg Glu Lys Lys Asp Arg 275 280 285 gtc ttc acc gac aag acc tca gcc acg gtc atc tgc cgc aaa aat gcc 3551 Val Phe Thr Asp Lys Thr Ser Ala Thr Val Ile Cys Arg Lys Asn Ala 290 295 300 agc att agc gtg cgg gcc cag gac cgc tac tat agc tca tct tgg agc 3599 Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr Tyr Ser Ser Ser Trp Ser 305 310 315 320 gaa tgg gca tct gtg ccc tgc agt cca tgg aga aac ctc ccc gtg gcc 3647 Glu Trp Ala Ser Val Pro Cys Ser Pro Trp Arg Asn Leu Pro Val Ala 325 330 335 act cca gac cca gga atg ttc cca tgc ctt cac cac tcc caa aac ctg 3695 Thr Pro Asp Pro Gly Met Phe Pro Cys Leu His His Ser Gln Asn Leu 340 345 350 ctg agg gcc gtc agc aac atg ctc cag aag gcc aga caa act cta gaa 3743 Leu Arg Ala Val Ser Asn Met Leu Gln Lys Ala Arg Gln Thr Leu Glu 355 360 365 ttt tac cct tgc act tct gaa gag att gat cat gaa gat atc aca aaa 3791 Phe Tyr Pro Cys Thr Ser Glu Glu Ile Asp His Glu Asp Ile Thr Lys 370 375 380 gat aaa acc agc aca gtg gag gcc tgt tta cca ttg gaa tta acc aag 3839 Asp Lys Thr Ser Thr Val Glu Ala Cys Leu Pro Leu Glu Leu Thr Lys 385 390 395 400 aat gag agt tgc cta aat tcc aga gag acc tct ttc ata act aat ggg 3887 Asn Glu Ser Cys Leu Asn Ser Arg Glu Thr Ser Phe Ile Thr Asn Gly 405 410 415 agt tgc ctg gcc tcc aga aag acc tct ttt atg atg gcc ctg tgc ctt 3935 Ser Cys Leu Ala Ser Arg Lys Thr Ser Phe Met Met Ala Leu Cys Leu 420 425 430 agt agt att tat gaa gac ttg aag atg tac cag gtg gag ttc aag acc 3983 Ser Ser Ile Tyr Glu Asp Leu Lys Met Tyr Gln Val Glu Phe Lys Thr 435 440 445 atg aat gca aag ctt ctg atg gat cct aag agg cag atc ttt cta gat 4031 Met Asn Ala Lys Leu Leu Met Asp Pro Lys Arg Gln Ile Phe Leu Asp 450 455 460 caa aac atg ctg gca gtt att gat gag ctg atg cag gcc ctg aat ttc 4079 Gln Asn Met Leu Ala Val Ile Asp Glu Leu Met Gln Ala Leu Asn Phe 465 470 475 480 aac agt gag act gtg cca caa aaa tcc tcc ctt gaa gaa ccg gat ttt 4127 Asn Ser Glu Thr Val Pro Gln Lys Ser Ser Leu Glu Glu Pro Asp Phe 485 490 495 tat aaa act aaa atc aag ctc tgc ata ctt ctt cat gct ttc aga att 4175 Tyr Lys Thr Lys Ile Lys Leu Cys Ile Leu Leu His Ala Phe Arg Ile 500 505 510 cgg gca gtg act att gat aga gtg atg agc tat ctg aat gct tcc taa 4223 Arg Ala Val Thr Ile Asp Arg Val Met Ser Tyr Leu Asn Ala Ser 515 520 525 aaagcgaggt gcggccgctt ccctttagtg agggttaatg cttcgagcag acatgataag 4283 atacattgat gagtttggac aaaccacaac tagaatgcag tgaaaaaaat gctttatttg 4343 tgaaatttgt gatgctattg ctttatttgt aaccattata agctgcaata aacaagttaa 4403 caacaacaat tgcattcatt ttatgtttca ggttcagggg gagatgtggg aggtttttta 4463 aagcaagtaa aacctctaca aatgtggtaa aatccgataa ggatcgatcc gggctggcgt 4523 aatagcgaag aggcccgcac cgatcgccct tcccaacagt tgcgcagcct gaatggcgaa 4583 tggacgcgcc ctgtagcggc gcattaagcg cggcgggtgt ggtggttacg cgcagcgtga 4643 ccgctacact tgccagcgcc ctagcgcccg ctcctttcgc tttcttccct tcctttctcg 4703 ccacgttcgc cggctttccc cgtcaagctc taaatcgggg gctcccttta gggttccgat 4763 ttagagcttt acggcacctc gaccgcaaaa aacttgattt gggtgatggt tcacgtagtg 4823 ggccatcgcc ctgatagacg gtttttcgcc ctttgacgtt ggagtccacg ttctttaata 4883 gtggactctt gttccaaact ggaacaacac tcaaccctat ctcggtctat tcttttgatt 4943 tataagggat tttgccgatt tcggcctatt ggttaaaaaa tgagctgatt taacaaatat 5003 ttaacgcgaa ttttaacaaa atattaacgt ttacaatttc gcctgatgcg gtattttctc 5063 cttacgcatc tgtgcggtat ttcacaccgc atacgcggat ctgcgcagca ccatggcctg 5123 aaataacctc tgaaagagga acttggttag gtaccttctg aggcggaaag aaccagctgt 5183 ggaatgtgtg tcagttaggg tgtggaaagt ccccaggctc cccagcaggc agaagtatgc 5243 aaagcatgca tctcaattag tcagcaacca ggtgtggaaa gtccccaggc tccccagcag 5303 gcagaagtat gcaaagcatg catctcaatt agtcagcaac catagtcccg cccctaactc 5363 cgcccatccc gcccctaact ccgcccagtt ccgcccattc tccgccccat ggctgactaa 5423 ttttttttat ttatgcagag gccgaggccg cctcggcctc tgagctattc cagaagtagt 5483 gaggaggctt ttttggaggc ctaggctttt gcaaaaagct tgattcttct gacacaacag 5543 tctcgaactt aaggctagag ccaccatgat tgaacaagat ggattgcacg caggttctcc 5603 ggccgcttgg gtggagaggc tattcggcta tgactgggca caacagacaa tcggctgctc 5663 tgatgccgcc gtgttccggc tgtcagcgca ggggcgcccg gttctttttg tcaagaccga 5723 cctgtccggt gccctgaatg aactgcagga cgaggcagcg cggctatcgt ggctggccac 5783 gacgggcgtt ccttgcgcag ctgtgctcga cgttgtcact gaagcgggaa gggactggct 5843 gctattgggc gaagtgccgg ggcaggatct cctgtcatct caccttgctc ctgccgagaa 5903 agtatccatc atggctgatg caatgcggcg gctgcatacg cttgatccgg ctacctgccc 5963 attcgaccac caagcgaaac atcgcatcga gcgagcacgt actcggatgg aagccggtct 6023 tgtcgatcag gatgatctgg acgaagagca tcaggggctc gcgccagccg aactgttcgc 6083 caggctcaag gcgcgcatgc ccgacggcga ggatctcgtc gtgacccatg gcgatgcctg 6143 cttgccgaat atcatggtgg aaaatggccg cttttctgga ttcatcgact gtggccggct 6203 gggtgtggcg gaccgctatc aggacatagc gttggctacc cgtgatattg ctgaagagct 6263 tggcggcgaa tgggctgacc gcttcctcgt gctttacggt atcgccgctc ccgattcgca 6323 gcgcatcgcc ttctatcgcc ttcttgacga gttcttctga gcgggactct ggggttcgaa 6383 atgaccgacc aagcgacgcc caacctgcca tcacgatggc cgcaataaaa tatctttatt 6443 ttcattacat ctgtgtgttg gttttttgtg tgaatcgata gcgataagga tccgcgtatg 6503 gtgcactctc agtacaatct gctctgatgc cgcatagtta agccagcccc gacacccgcc 6563 aacacccgct gacgcgccct gacgggcttg tctgctcccg gcatccgctt acagacaagc 6623 tgtgaccgtc tccgggagct gcatgtgtca gaggttttca ccgtcatcac cgaaacgcgc 6683 gagacgaaag ggcctcgtga tacgcctatt tttataggtt aatgtcatga taataatggt 6743 ttcttagacg tcaggtggca cttttcgggg aaatgtgcgc ggaaccccta tttgtttatt 6803 tttctaaata cattcaaata tgtatccgct catgagacaa taaccctgat aaatgcttca 6863 ataatattga aaaaggaaga gtatgagtat tcaacatttc cgtgtcgccc ttattccctt 6923 ttttgcggca ttttgccttc ctgtttttgc tcacccagaa acgctggtga aagtaaaaga 6983 tgctgaagat cagttgggtg cacgagtggg ttacatcgaa ctggatctca acagcggtaa 7043 gatccttgag agttttcgcc ccgaagaacg ttttccaatg atgagcactt ttaaagttct 7103 gctatgtggc gcggtattat cccgtattga cgccgggcaa gagcaactcg gtcgccgcat 7163 acactattct cagaatgact tggttgagta ctcaccagtc acagaaaagc atcttacgga 7223 tggcatgaca gtaagagaat tatgcagtgc tgccataacc atgagtgata acactgcggc 7283 caacttactt ctgacaacga tcggaggacc gaaggagcta accgcttttt tgcacaacat 7343 gggggatcat gtaactcgcc ttgatcgttg ggaaccggag ctgaatgaag ccataccaaa 7403 cgacgagcgt gacaccacga tgcctgtagc aatggcaaca acgttgcgca aactattaac 7463 tggcgaacta cttactctag cttcccggca acaattaata gactggatgg aggcggataa 7523 agttgcagga ccacttctgc gctcggccct tccggctggc tggtttattg ctgataaatc 7583 tggagccggt gagcgtgggt ctcgcggtat cattgcagca ctggggccag atggtaagcc 7643 ctcccgtatc gtagttatct acacgacggg gagtcaggca actatggatg aacgaaatag 7703 acagatcgct gagataggtg cctcactgat taagcattgg taactgtcag accaagttta 7763 ctcatatata ctttagattg atttaaaact tcatttttaa tttaaaagga tctaggtgaa 7823 gatccttttt gataatctca tgaccaaaat cccttaacgt gagttttcgt tccactgagc 7883 gtcagacccc gtagaaaaga tcaaaggatc ttcttgagat cctttttttc tgcgcgtaat 7943 ctgctgcttg caaacaaaaa aaccaccgct accagcggtg gtttgtttgc cggatcaaga 8003 gctaccaact ctttttccga aggtaactgg cttcagcaga gcgcagatac caaatactgt 8063 ccttctagtg tagccgtagt taggccacca cttcaagaac tctgtagcac cgcctacata 8123 cctcgctctg ctaatcctgt taccagtggc tgctgccagt ggcgataagt cgtgtcttac 8183 cgggttggac tcaagacgat agttaccgga taaggcgcag cggtcgggct gaacgggggg 8243 ttcgtgcaca cagcccagct tggagcgaac gacctacacc gaactgagat acctacagcg 8303 tgagctatga gaaagcgcca cgcttcccga agggagaaag gcggacaggt atccggtaag 8363 cggcagggtc ggaacaggag agcgcacgag ggagcttcca gggggaaacg cctggtatct 8423 ttatagtcct gtcgggtttc gccacctctg acttgagcgt cgatttttgt gatgctcgtc 8483 aggggggcgg agcctatgga aaaacgccag caacgcggcc tttttacggt tcctggcctt 8543 ttgctggcct tttgctcaca tggctcgaca gatct 8578 2 527 PRT Artificial Sequence Description of Artificial Sequence Plasmid 2 Met Cys His Gln Gln Leu Val Ile Ser Trp Phe Ser Leu Val Phe Leu 1 5 10 15 Ala Ser Pro Leu Val Ala Ile Trp Glu Leu Lys Lys Asp Val Tyr Val 20 25 30 Val Glu Leu Asp Trp Tyr Pro Asp Ala Pro Gly Glu Met Val Val Leu 35 40 45 Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile Thr Trp Thr Leu Asp Gln 50 55 60 Ser Ser Glu Val Leu Gly Ser Gly Lys Thr Leu Thr Ile Gln Val Lys 65 70 75 80 Glu Phe Gly Asp Ala Gly Gln Tyr Thr Cys His Lys Gly Gly Glu Val 85 90 95 Leu Ser His Ser Leu Leu Leu Leu His Lys Lys Glu Asp Gly Ile Trp 100 105 110 Ser Thr Asp Ile Leu Lys Asp Gln Lys Glu Pro Lys Asn Lys Thr Phe 115 120 125 Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly Arg Phe Thr Cys Trp Trp 130 135 140 Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe Ser Val Lys Ser Ser Arg 145 150 155 160 Gly Ser Ser Asp Pro Gln Gly Val Thr Cys Gly Ala Ala Thr Leu Ser 165 170 175 Ala Glu Arg Val Arg Gly Asp Asn Lys Glu Tyr Glu Tyr Ser Val Glu 180 185 190 Cys Gln Glu Asp Ser Ala Cys Pro Ala Ala Glu Glu Ser Leu Pro Ile 195 200 205 Glu Val Met Val Asp Ala Val His Lys Leu Lys Tyr Glu Asn Tyr Thr 210 215 220 Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys Pro Asp Pro Pro Asn Asn 225 230 235 240 Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg Gln Val Glu Val Ser Trp 245 250 255 Glu Tyr Pro Asp Thr Trp Ser Thr Pro His Ser Tyr Phe Ser Leu Thr 260 265 270 Phe Cys Val Gln Val Gln Gly Lys Ser Lys Arg Glu Lys Lys Asp Arg 275 280 285 Val Phe Thr Asp Lys Thr Ser Ala Thr Val Ile Cys Arg Lys Asn Ala 290 295 300 Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr Tyr Ser Ser Ser Trp Ser 305 310 315 320 Glu Trp Ala Ser Val Pro Cys Ser Pro Trp Arg Asn Leu Pro Val Ala 325 330 335 Thr Pro Asp Pro Gly Met Phe Pro Cys Leu His His Ser Gln Asn Leu 340 345 350 Leu Arg Ala Val Ser Asn Met Leu Gln Lys Ala Arg Gln Thr Leu Glu 355 360 365 Phe Tyr Pro Cys Thr Ser Glu Glu Ile Asp His Glu Asp Ile Thr Lys 370 375 380 Asp Lys Thr Ser Thr Val Glu Ala Cys Leu Pro Leu Glu Leu Thr Lys 385 390 395 400 Asn Glu Ser Cys Leu Asn Ser Arg Glu Thr Ser Phe Ile Thr Asn Gly 405 410 415 Ser Cys Leu Ala Ser Arg Lys Thr Ser Phe Met Met Ala Leu Cys Leu 420 425 430 Ser Ser Ile Tyr Glu Asp Leu Lys Met Tyr Gln Val Glu Phe Lys Thr 435 440 445 Met Asn Ala Lys Leu Leu Met Asp Pro Lys Arg Gln Ile Phe Leu Asp 450 455 460 Gln Asn Met Leu Ala Val Ile Asp Glu Leu Met Gln Ala Leu Asn Phe 465 470 475 480 Asn Ser Glu Thr Val Pro Gln Lys Ser Ser Leu Glu Glu Pro Asp Phe 485 490 495 Tyr Lys Thr Lys Ile Lys Leu Cys Ile Leu Leu His Ala Phe Arg Ile 500 505 510 Arg Ala Val Thr Ile Asp Arg Val Met Ser Tyr Leu Asn Ala Ser 515 520 525 3 8578 DNA Artificial Sequence Description of Artificial Sequence plasmid 3 tcaatattgg ccattagcca tattattcat tggttatata gcataaatca atattggcta 60 ttggccattg catacgttgt atctatatca taatatgtac atttatattg gctcatgtcc 120 aatatgaccg ccatgttggc attgattatt gactagttat taatagtaat caattacggg 180 gtcattagtt catagcccat atatggagtt ccgcgttaca taacttacgg taaatggccc 240 gcctggctga ccgcccaacg acccccgccc attgacgtca ataatgacgt atgttcccat 300 agtaacgcca atagggactt tccattgacg tcaatgggtg gagtatttac ggtaaactgc 360 ccacttggca gtacatcaag tgtatcatat gccaagtccg ccccctattg acgtcaatga 420 cggtaaatgg cccgcctggc attatgccca gtacatgacc ttacgggact ttcctacttg 480 gcagtacatc tacgtattag tcatcgctat taccatggtg atgcggtttt ggcagtacac 540 caatgggcgt ggatagcggt ttgactcacg gggatttcca agtctccacc ccattgacgt 600 caatgggagt ttgttttggc accaaaatca acgggacttt ccaaaatgtc gtaacaactg 660 cgatcgcccg ccccgttgac gcaaatgggc ggtaggcgtg tacggtggga ggtctatata 720 agcagagctc gtttagtgaa ccgtcagatc actagaagct ttattgcggt agtttatcac 780 agttaaattg ctaacgcagt cagtgcttct gacacaacag tctcgaactt aagctgcagt 840 gactctctta aggtagcctt gcagaagttg gtcgtgaggc actgggcagg taagtatcaa 900 ggttacaaga caggtttaag gagaccaata gaaactgggc ttgtcgagac agagaagact 960 cttgcgtttc tgataggcac ctattggtct tactgacatc cactttgcct ttctctccac 1020 aggtgtccac tcccagttca attacagctc ttaaggctag agtacttaat acgactcact 1080 ataggctaga tgggccacac acggaggcag ggaacatcac catccaagtg tccatacctc 1140 aatttctttc agctcttggt gctggctggt ctttctcact tctgttcagg tgttatccac 1200 gtgaccaagg aagtgaaaga agtggcaacg ctgtcctgtg gtcacaatgt ttctgttgaa 1260 gagctggcac aaactcgcat ctactggcaa aaggagaaga aaatggtgct gactatgatg 1320 tctggggaca tgaatatatg gcccgagtac aagaaccgga ccatctttga tatcactaat 1380 aacctctcca ttgtgatcct ggctctgcgc ccatctgacg agggcacata cgagtgtgtt 1440 gttctgaagt atgaaaaaga cgctttcaag cgggaacacc tggctgaagt gacgttatca 1500 gtcaaagctg acttccctac acctagtata tctgactttg aaattccaac ttctaatatt 1560 agaaggataa tttgctcaac ctctggaggt tttccagagc ctcacctctc ctggttggaa 1620 aatggagaag aattaaatgc catcaacaca acagtttccc aagatcctga aactgagctc 1680 tatgctgtta gcagcaaact ggatttcaat atgacaacca accacagctt catgtgtctc 1740 atcaagtatg gacatttaag agtgaatcag accttcaact ggaatacaac caagcaagag 1800 cattttcctg ataacctgct cccatcctgg gccattacct taatctcagt aaatggaatt 1860 tttgtgatat gctgcctgac ctactgcttt gccccaagat gcagagagag aaggaggaat 1920 gagagattga gaagggaaag tgtacgccct gtataacagt gtccgcagaa gcaaggggct 1980 gaaaacgcgt cgagcatgca tctagggcgg ccaattccgc ccctctccct cccccccccc 2040 taacgttact ggccgaagcc gcttggaata aggccggtgt gcgtttgtct atatgtgatt 2100 ttccaccata ttgccgtctt ttggcaatgt gagggcccgg aaacctggcc ctgtcttctt 2160 gacgagcatt cctaggggtc tttcccctct cgccaaagga atgcaaggtc tgttgaatgt 2220 cgtgaaggaa gcagttcctc tggaagcttc ttgaagacaa acaacgtctg tagcgaccct 2280 ttgcaggcag cggaaccccc cacctggcga caggtgcctc tgcggccaaa agccacgtgt 2340 ataagataca cctgcaaagg cggcacaacc ccagtgccac gttgtgagtt ggatagttgt 2400 ggaaagagtc aaatggctct cctcaagcgt attcaacaag gggctgaagg atgcccagaa 2460 ggtaccccat tgtatgggat ctgatctggg gcctcggtgc acatgcttta catgtgttta 2520 gtcgaggtta aaaaaacgtc taggcccccc gaaccacggg gacgtggttt tcctttgaaa 2580 aacacgatga taagcttgcc acaacccggg atcctctaga gtcgacggcc cagagcaag 2639 atg tgt cac cag cag ttg gtc atc tct tgg ttt tcc ctg gtt ttt ctg 2687 Met Cys His Gln Gln Leu Val Ile Ser Trp Phe Ser Leu Val Phe Leu 1 5 10 15 gca tct ccc ctc gtg gcc ata tgg gaa ctg aag aaa gat gtt tat gtc 2735 Ala Ser Pro Leu Val Ala Ile Trp Glu Leu Lys Lys Asp Val Tyr Val 20 25 30 gta gaa ttg gat tgg tat ccg gat gcc cct gga gaa atg gtg gtc ctc 2783 Val Glu Leu Asp Trp Tyr Pro Asp Ala Pro Gly Glu Met Val Val Leu 35 40 45 acc tgt gac acc cct gaa gaa gat ggt atc acc tgg acc ttg gac cag 2831 Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile Thr Trp Thr Leu Asp Gln 50 55 60 agc agt gag gtc tta ggc tct ggc aaa acc ctg acc atc caa gtc aaa 2879 Ser Ser Glu Val Leu Gly Ser Gly Lys Thr Leu Thr Ile Gln Val Lys 65 70 75 80 gag ttt gga gat gct ggc cag tac acc tgt cac aaa gga ggc gag gtt 2927 Glu Phe Gly Asp Ala Gly Gln Tyr Thr Cys His Lys Gly Gly Glu Val 85 90 95 cta agc cat tcg ctc ctg ctg ctt cac aaa aag gaa gat gga att tgg 2975 Leu Ser His Ser Leu Leu Leu Leu His Lys Lys Glu Asp Gly Ile Trp 100 105 110 tcc act gat att tta aag gac cag aaa gaa ccc aaa aat aag acc ttt 3023 Ser Thr Asp Ile Leu Lys Asp Gln Lys Glu Pro Lys Asn Lys Thr Phe 115 120 125 cta aga tgc gag gcc aag aat tat tct gga cgt ttc acc tgc tgg tgg 3071 Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly Arg Phe Thr Cys Trp Trp 130 135 140 ctg acg aca atc agt act gat ttg aca ttc agt gtc aaa agc agc aga 3119 Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe Ser Val Lys Ser Ser Arg 145 150 155 160 ggc tct tct gac ccc caa ggg gtg acg tgc gga gct gct aca ctc tct 3167 Gly Ser Ser Asp Pro Gln Gly Val Thr Cys Gly Ala Ala Thr Leu Ser 165 170 175 gca gag aga gtc aga ggg gac aac aag gag tat gag tac tca gtg gag 3215 Ala Glu Arg Val Arg Gly Asp Asn Lys Glu Tyr Glu Tyr Ser Val Glu 180 185 190 tgc cag gag gac agt gcc tgc cca gct gct gag gag agt ctg ccc att 3263 Cys Gln Glu Asp Ser Ala Cys Pro Ala Ala Glu Glu Ser Leu Pro Ile 195 200 205 gag gtc atg gtg gat gcc gtt cac aag ctc aag tat gaa aac tac acc 3311 Glu Val Met Val Asp Ala Val His Lys Leu Lys Tyr Glu Asn Tyr Thr 210 215 220 agc agc ttc ttc atc agg gac atc atc aaa cct gac cca ccc aac aac 3359 Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys Pro Asp Pro Pro Asn Asn 225 230 235 240 ttg cag ctg aag cca tta aag aat tct cgg cag gtg gag gtc agc tgg 3407 Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg Gln Val Glu Val Ser Trp 245 250 255 gag tac cct gac acc tgg agt act cca cat tcc tac ttc tcc ctg aca 3455 Glu Tyr Pro Asp Thr Trp Ser Thr Pro His Ser Tyr Phe Ser Leu Thr 260 265 270 ttc tgc gtt cag gtc cag ggc aag agc aag aga gaa aag aaa gat aga 3503 Phe Cys Val Gln Val Gln Gly Lys Ser Lys Arg Glu Lys Lys Asp Arg 275 280 285 gtc ttc acc gac aag acc tca gcc acg gtc atc tgc cgc aaa aat gcc 3551 Val Phe Thr Asp Lys Thr Ser Ala Thr Val Ile Cys Arg Lys Asn Ala 290 295 300 agc att agc gtg cgg gcc cag gac cgc tac tat agc tca tct tgg agc 3599 Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr Tyr Ser Ser Ser Trp Ser 305 310 315 320 gaa tgg gca tct gtg ccc tgc agt cca tgg aga aac ctc ccc gtg gcc 3647 Glu Trp Ala Ser Val Pro Cys Ser Pro Trp Arg Asn Leu Pro Val Ala 325 330 335 act cca gac cca gga atg ttc cca tgc ctt cac cac tcc caa aac ctg 3695 Thr Pro Asp Pro Gly Met Phe Pro Cys Leu His His Ser Gln Asn Leu 340 345 350 ctg agg gcc gtc agc aac atg ctc cag aag gcc aga caa act cta gaa 3743 Leu Arg Ala Val Ser Asn Met Leu Gln Lys Ala Arg Gln Thr Leu Glu 355 360 365 ttt tac cct tgc act tct gaa gag att gat cat gaa gat atc aca aaa 3791 Phe Tyr Pro Cys Thr Ser Glu Glu Ile Asp His Glu Asp Ile Thr Lys 370 375 380 gat aaa acc agc aca gtg gag gcc tgt tta cca ttg gaa tta acc aag 3839 Asp Lys Thr Ser Thr Val Glu Ala Cys Leu Pro Leu Glu Leu Thr Lys 385 390 395 400 aat gag agt tgc cta aat tcc aga gag acc tct ttc ata act aat ggg 3887 Asn Glu Ser Cys Leu Asn Ser Arg Glu Thr Ser Phe Ile Thr Asn Gly 405 410 415 agt tgc ctg gcc tcc aga aag acc tct ttt atg atg gcc ctg tgc ctt 3935 Ser Cys Leu Ala Ser Arg Lys Thr Ser Phe Met Met Ala Leu Cys Leu 420 425 430 agt agt att tat gaa gac ttg aag atg tac cag gtg gag ttc aag acc 3983 Ser Ser Ile Tyr Glu Asp Leu Lys Met Tyr Gln Val Glu Phe Lys Thr 435 440 445 atg aat gca aag ctt ctg atg gat cct aag agg cag atc ttt cta gat 4031 Met Asn Ala Lys Leu Leu Met Asp Pro Lys Arg Gln Ile Phe Leu Asp 450 455 460 caa aac atg ctg gca gtt att gat gag ctg atg cag gcc ctg aat ttc 4079 Gln Asn Met Leu Ala Val Ile Asp Glu Leu Met Gln Ala Leu Asn Phe 465 470 475 480 aac agt gag act gtg cca caa aaa tcc tcc ctt gaa gaa ccg gat ttt 4127 Asn Ser Glu Thr Val Pro Gln Lys Ser Ser Leu Glu Glu Pro Asp Phe 485 490 495 tat aaa act aaa atc aag ctc tgc ata ctt ctt cat gct ttc aga att 4175 Tyr Lys Thr Lys Ile Lys Leu Cys Ile Leu Leu His Ala Phe Arg Ile 500 505 510 cgg gca gtg act att gat aga gtg atg agc tat ctg aat gct 4217 Arg Ala Val Thr Ile Asp Arg Val Met Ser Tyr Leu Asn Ala 515 520 525 tcctaaaaag cgaggtgcgg ccgcttccct ttagtgaggg ttaatgcttc gagcagacat 4277 gataagatac attgatgagt ttggacaaac cacaactaga atgcagtgaa aaaaatgctt 4337 tatttgtgaa atttgtgatg ctattgcttt atttgtaacc attataagct gcaataaaca 4397 agttaacaac aacaattgca ttcattttat gtttcaggtt cagggggaga tgtgggaggt 4457 tttttaaagc aagtaaaacc tctacaaatg tggtaaaatc cgataaggat cgatccgggc 4517 tggcgtaata gcgaagaggc ccgcaccgat cgcccttccc aacagttgcg cagcctgaat 4577 ggcgaatgga cgcgccctgt agcggcgcat taagcgcggc gggtgtggtg gttacgcgca 4637 gcgtgaccgc tacacttgcc agcgccctag cgcccgctcc tttcgctttc ttcccttcct 4697 ttctcgccac gttcgccggc tttccccgtc aagctctaaa tcgggggctc cctttagggt 4757 tccgatttag agctttacgg cacctcgacc gcaaaaaact tgatttgggt gatggttcac 4817 gtagtgggcc atcgccctga tagacggttt ttcgcccttt gacgttggag tccacgttct 4877 ttaatagtgg actcttgttc caaactggaa caacactcaa ccctatctcg gtctattctt 4937 ttgatttata agggattttg ccgatttcgg cctattggtt aaaaaatgag ctgatttaac 4997 aaatatttaa cgcgaatttt aacaaaatat taacgtttac aatttcgcct gatgcggtat 5057 tttctcctta cgcatctgtg cggtatttca caccgcatac gcggatctgc gcagcaccat 5117 ggcctgaaat aacctctgaa agaggaactt ggttaggtac cttctgaggc ggaaagaacc 5177 agctgtggaa tgtgtgtcag ttagggtgtg gaaagtcccc aggctcccca gcaggcagaa 5237 gtatgcaaag catgcatctc aattagtcag caaccaggtg tggaaagtcc ccaggctccc 5297 cagcaggcag aagtatgcaa agcatgcatc tcaattagtc agcaaccata gtcccgcccc 5357 taactccgcc catcccgccc ctaactccgc ccagttccgc ccattctccg ccccatggct 5417 gactaatttt ttttatttat gcagaggccg aggccgcctc ggcctctgag ctattccaga 5477 agtagtgagg aggctttttt ggaggcctag gcttttgcaa aaagcttgat tcttctgaca 5537 caacagtctc gaacttaagg ctagagccac catgattgaa caagatggat tgcacgcagg 5597 ttctccggcc gcttgggtgg agaggctatt cggctatgac tgggcacaac agacaatcgg 5657 ctgctctgat gccgccgtgt tccggctgtc agcgcagggg cgcccggttc tttttgtcaa 5717 gaccgacctg tccggtgccc tgaatgaact gcaggacgag gcagcgcggc tatcgtggct 5777 ggccacgacg ggcgttcctt gcgcagctgt gctcgacgtt gtcactgaag cgggaaggga 5837 ctggctgcta ttgggcgaag tgccggggca ggatctcctg tcatctcacc ttgctcctgc 5897 cgagaaagta tccatcatgg ctgatgcaat gcggcggctg catacgcttg atccggctac 5957 ctgcccattc gaccaccaag cgaaacatcg catcgagcga gcacgtactc ggatggaagc 6017 cggtcttgtc gatcaggatg atctggacga agagcatcag gggctcgcgc cagccgaact 6077 gttcgccagg ctcaaggcgc gcatgcccga cggcgaggat ctcgtcgtga cccatggcga 6137 tgcctgcttg ccgaatatca tggtggaaaa tggccgcttt tctggattca tcgactgtgg 6197 ccggctgggt gtggcggacc gctatcagga catagcgttg gctacccgtg atattgctga 6257 agagcttggc ggcgaatggg ctgaccgctt cctcgtgctt tacggtatcg ccgctcccga 6317 ttcgcagcgc atcgccttct atcgccttct tgacgagttc ttctgagcgg gactctgggg 6377 ttcgaaatga ccgaccaagc gacgcccaac ctgccatcac gatggccgca ataaaatatc 6437 tttattttca ttacatctgt gtgttggttt tttgtgtgaa tcgatagcga taaggatccg 6497 cgtatggtgc actctcagta caatctgctc tgatgccgca tagttaagcc agccccgaca 6557 cccgccaaca cccgctgacg cgccctgacg ggcttgtctg ctcccggcat ccgcttacag 6617 acaagctgtg accgtctccg ggagctgcat gtgtcagagg ttttcaccgt catcaccgaa 6677 acgcgcgaga cgaaagggcc tcgtgatacg cctattttta taggttaatg tcatgataat 6737 aatggtttct tagacgtcag gtggcacttt tcggggaaat gtgcgcggaa cccctatttg 6797 tttatttttc taaatacatt caaatatgta tccgctcatg agacaataac cctgataaat 6857 gcttcaataa tattgaaaaa ggaagagtat gagtattcaa catttccgtg tcgcccttat 6917 tccctttttt gcggcatttt gccttcctgt ttttgctcac ccagaaacgc tggtgaaagt 6977 aaaagatgct gaagatcagt tgggtgcacg agtgggttac atcgaactgg atctcaacag 7037 cggtaagatc cttgagagtt ttcgccccga agaacgtttt ccaatgatga gcacttttaa 7097 agttctgcta tgtggcgcgg tattatcccg tattgacgcc gggcaagagc aactcggtcg 7157 ccgcatacac tattctcaga atgacttggt tgagtactca ccagtcacag aaaagcatct 7217 tacggatggc atgacagtaa gagaattatg cagtgctgcc ataaccatga gtgataacac 7277 tgcggccaac ttacttctga caacgatcgg aggaccgaag gagctaaccg cttttttgca 7337 caacatgggg gatcatgtaa ctcgccttga tcgttgggaa ccggagctga atgaagccat 7397 accaaacgac gagcgtgaca ccacgatgcc tgtagcaatg gcaacaacgt tgcgcaaact 7457 attaactggc gaactactta ctctagcttc ccggcaacaa ttaatagact ggatggaggc 7517 ggataaagtt gcaggaccac ttctgcgctc ggcccttccg gctggctggt ttattgctga 7577 taaatctgga gccggtgagc gtgggtctcg cggtatcatt gcagcactgg ggccagatgg 7637 taagccctcc cgtatcgtag ttatctacac gacggggagt caggcaacta tggatgaacg 7697 aaatagacag atcgctgaga taggtgcctc actgattaag cattggtaac tgtcagacca 7757 agtttactca tatatacttt agattgattt aaaacttcat ttttaattta aaaggatcta 7817 ggtgaagatc ctttttgata atctcatgac caaaatccct taacgtgagt tttcgttcca 7877 ctgagcgtca gaccccgtag aaaagatcaa aggatcttct tgagatcctt tttttctgcg 7937 cgtaatctgc tgcttgcaaa caaaaaaacc accgctacca gcggtggttt gtttgccgga 7997 tcaagagcta ccaactcttt ttccgaaggt aactggcttc agcagagcgc agataccaaa 8057 tactgtcctt ctagtgtagc cgtagttagg ccaccacttc aagaactctg tagcaccgcc 8117 tacatacctc gctctgctaa tcctgttacc agtggctgct gccagtggcg ataagtcgtg 8177 tcttaccggg ttggactcaa gacgatagtt accggataag gcgcagcggt cgggctgaac 8237 ggggggttcg tgcacacagc ccagcttgga gcgaacgacc tacaccgaac tgagatacct 8297 acagcgtgag ctatgagaaa gcgccacgct tcccgaaggg agaaaggcgg acaggtatcc 8357 ggtaagcggc agggtcggaa caggagagcg cacgagggag cttccagggg gaaacgcctg 8417 gtatctttat agtcctgtcg ggtttcgcca cctctgactt gagcgtcgat ttttgtgatg 8477 ctcgtcaggg gggcggagcc tatggaaaaa cgccagcaac gcggcctttt tacggttcct 8537 ggccttttgc tggccttttg ctcacatggc tcgacagatc t 8578 4 526 PRT Artificial Sequence Description of Artificial Sequence plasmid 4 Met Cys His Gln Gln Leu Val Ile Ser Trp Phe Ser Leu Val Phe Leu 1 5 10 15 Ala Ser Pro Leu Val Ala Ile Trp Glu Leu Lys Lys Asp Val Tyr Val 20 25 30 Val Glu Leu Asp Trp Tyr Pro Asp Ala Pro Gly Glu Met Val Val Leu 35 40 45 Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile Thr Trp Thr Leu Asp Gln 50 55 60 Ser Ser Glu Val Leu Gly Ser Gly Lys Thr Leu Thr Ile Gln Val Lys 65 70 75 80 Glu Phe Gly Asp Ala Gly Gln Tyr Thr Cys His Lys Gly Gly Glu Val 85 90 95 Leu Ser His Ser Leu Leu Leu Leu His Lys Lys Glu Asp Gly Ile Trp 100 105 110 Ser Thr Asp Ile Leu Lys Asp Gln Lys Glu Pro Lys Asn Lys Thr Phe 115 120 125 Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly Arg Phe Thr Cys Trp Trp 130 135 140 Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe Ser Val Lys Ser Ser Arg 145 150 155 160 Gly Ser Ser Asp Pro Gln Gly Val Thr Cys Gly Ala Ala Thr Leu Ser 165 170 175 Ala Glu Arg Val Arg Gly Asp Asn Lys Glu Tyr Glu Tyr Ser Val Glu 180 185 190 Cys Gln Glu Asp Ser Ala Cys Pro Ala Ala Glu Glu Ser Leu Pro Ile 195 200 205 Glu Val Met Val Asp Ala Val His Lys Leu Lys Tyr Glu Asn Tyr Thr 210 215 220 Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys Pro Asp Pro Pro Asn Asn 225 230 235 240 Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg Gln Val Glu Val Ser Trp 245 250 255 Glu Tyr Pro Asp Thr Trp Ser Thr Pro His Ser Tyr Phe Ser Leu Thr 260 265 270 Phe Cys Val Gln Val Gln Gly Lys Ser Lys Arg Glu Lys Lys Asp Arg 275 280 285 Val Phe Thr Asp Lys Thr Ser Ala Thr Val Ile Cys Arg Lys Asn Ala 290 295 300 Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr Tyr Ser Ser Ser Trp Ser 305 310 315 320 Glu Trp Ala Ser Val Pro Cys Ser Pro Trp Arg Asn Leu Pro Val Ala 325 330 335 Thr Pro Asp Pro Gly Met Phe Pro Cys Leu His His Ser Gln Asn Leu 340 345 350 Leu Arg Ala Val Ser Asn Met Leu Gln Lys Ala Arg Gln Thr Leu Glu 355 360 365 Phe Tyr Pro Cys Thr Ser Glu Glu Ile Asp His Glu Asp Ile Thr Lys 370 375 380 Asp Lys Thr Ser Thr Val Glu Ala Cys Leu Pro Leu Glu Leu Thr Lys 385 390 395 400 Asn Glu Ser Cys Leu Asn Ser Arg Glu Thr Ser Phe Ile Thr Asn Gly 405 410 415 Ser Cys Leu Ala Ser Arg Lys Thr Ser Phe Met Met Ala Leu Cys Leu 420 425 430 Ser Ser Ile Tyr Glu Asp Leu Lys Met Tyr Gln Val Glu Phe Lys Thr 435 440 445 Met Asn Ala Lys Leu Leu Met Asp Pro Lys Arg Gln Ile Phe Leu Asp 450 455 460 Gln Asn Met Leu Ala Val Ile Asp Glu Leu Met Gln Ala Leu Asn Phe 465 470 475 480 Asn Ser Glu Thr Val Pro Gln Lys Ser Ser Leu Glu Glu Pro Asp Phe 485 490 495 Tyr Lys Thr Lys Ile Lys Leu Cys Ile Leu Leu His Ala Phe Arg Ile 500 505 510 Arg Ala Val Thr Ile Asp Arg Val Met Ser Tyr Leu Asn Ala 515 520 525 5 8623 DNA Artificial Sequence misc_feature (1)..(750) CMV enhancer and promoter 5 tcaatattgg ccattagcca tattattcat tggttatata gcataaatca atattggcta 60 ttggccattg catacgttgt atctatatca taatatgtac atttatattg gctcatgtcc 120 aatatgaccg ccatgttggc attgattatt gactagttat taatagtaat caattacggg 180 gtcattagtt catagcccat atatggagtt ccgcgttaca taacttacgg taaatggccc 240 gcctggctga ccgcccaacg acccccgccc attgacgtca ataatgacgt atgttcccat 300 agtaacgcca atagggactt tccattgacg tcaatgggtg gagtatttac ggtaaactgc 360 ccacttggca gtacatcaag tgtatcatat gccaagtccg ccccctattg acgtcaatga 420 cggtaaatgg cccgcctggc attatgccca gtacatgacc ttacgggact ttcctacttg 480 gcagtacatc tacgtattag tcatcgctat taccatggtg atgcggtttt ggcagtacac 540 caatgggcgt ggatagcggt ttgactcacg gggatttcca agtctccacc ccattgacgt 600 caatgggagt ttgttttggc accaaaatca acgggacttt ccaaaatgtc gtaacaactg 660 cgatcgcccg ccccgttgac gcaaatgggc ggtaggcgtg tacggtggga ggtctatata 720 agcagagctc gtttagtgaa ccgtcagatc actagaagct ttattgcggt agtttatcac 780 agttaaattg ctaacgcagt cagtgcttct gacacaacag tctcgaactt aagctgcagt 840 gactctctta aggtagcctt gcagaagttg gtcgtgaggc actgggcagg taagtatcaa 900 ggttacaaga caggtttaag gagaccaata gaaactgggc ttgtcgagac agagaagact 960 cttgcgtttc tgataggcac ctattggtct tactgacatc cactttgcct ttctctccac 1020 aggtgtccac tcccagttca attacagctc ttaaggctag agtacttaat acgactcact 1080 ataggctaga tgggccacac acggaggcag ggaacatcac catccaagtg tccatacctc 1140 aatttctttc agctcttggt gctggctggt ctttctcact tctgttcagg tgttatccac 1200 gtgaccaagg aagtgaaaga agtggcaacg ctgtcctgtg gtcacaatgt ttctgttgaa 1260 gagctggcac aaactcgcat ctactggcaa aaggagaaga aaatggtgct gactatgatg 1320 tctggggaca tgaatatatg gcccgagtac aagaaccgga ccatctttga tatcactaat 1380 aacctctcca ttgtgatcct ggctctgcgc ccatctgacg agggcacata cgagtgtgtt 1440 gttctgaagt atgaaaaaga cgctttcaag cgggaacacc tggctgaagt gacgttatca 1500 gtcaaagctg acttccctac acctagtata tctgactttg aaattccaac ttctaatatt 1560 agaaggataa tttgctcaac ctctggaggt tttccagagc ctcacctctc ctggttggaa 1620 aatggagaag aattaaatgc catcaacaca acagtttccc aagatcctga aactgagctc 1680 tatgctgtta gcagcaaact ggatttcaat atgacaacca accacagctt catgtgtctc 1740 atcaagtatg gacatttaag agtgaatcag accttcaact ggaatacaac caagcaagag 1800 cattttcctg ataacctgct cccatcctgg gccattacct taatctcagt aaatggaatt 1860 tttgtgatat gctgcctgac ctactgcttt gccccaagat gcagagagag aaggaggaat 1920 gagagattga gaagggaaag tgtacgccct gtataacagt gtccgcagaa gcaaggggct 1980 gaaaacgcgt cgagcatgca tctagggcgg ccaattccgc ccctctccct cccccccccc 2040 taacgttact ggccgaagcc gcttggaata aggccggtgt gcgtttgtct atatgtgatt 2100 ttccaccata ttgccgtctt ttggcaatgt gagggcccgg aaacctggcc ctgtcttctt 2160 gacgagcatt cctaggggtc tttcccctct cgccaaagga atgcaaggtc tgttgaatgt 2220 cgtgaaggaa gcagttcctc tggaagcttc ttgaagacaa acaacgtctg tagcgaccct 2280 ttgcaggcag cggaaccccc cacctggcga caggtgcctc tgcggccaaa agccacgtgt 2340 ataagataca cctgcaaagg cggcacaacc ccagtgccac gttgtgagtt ggatagttgt 2400 ggaaagagtc aaatggctct cctcaagcgt attcaacaag gggctgaagg atgcccagaa 2460 ggtaccccat tgtatgggat ctgatctggg gcctcggtgc acatgcttta catgtgttta 2520 gtcgaggtta aaaaaacgtc taggcccccc gaaccacggg gacgtggttt tcctttgaaa 2580 aacacgatga taagcttgcc acaacccggg atcctctaga gtcgacggcc cagagcaag 2639 atg tgt cac cag cag ttg gtc atc tct tgg ttt tcc ctg gtt ttt ctg 2687 Met Cys His Gln Gln Leu Val Ile Ser Trp Phe Ser Leu Val Phe Leu 1 5 10 15 gca tct ccc ctc gtg gcc ata tgg gaa ctg aag aaa gat gtt tat gtc 2735 Ala Ser Pro Leu Val Ala Ile Trp Glu Leu Lys Lys Asp Val Tyr Val 20 25 30 gta gaa ttg gat tgg tat ccg gat gcc cct gga gaa atg gtg gtc ctc 2783 Val Glu Leu Asp Trp Tyr Pro Asp Ala Pro Gly Glu Met Val Val Leu 35 40 45 acc tgt gac acc cct gaa gaa gat ggt atc acc tgg acc ttg gac cag 2831 Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile Thr Trp Thr Leu Asp Gln 50 55 60 agc agt gag gtc tta ggc tct ggc aaa acc ctg acc atc caa gtc aaa 2879 Ser Ser Glu Val Leu Gly Ser Gly Lys Thr Leu Thr Ile Gln Val Lys 65 70 75 80 gag ttt gga gat gct ggc cag tac acc tgt cac aaa gga ggc gag gtt 2927 Glu Phe Gly Asp Ala Gly Gln Tyr Thr Cys His Lys Gly Gly Glu Val 85 90 95 cta agc cat tcg ctc ctg ctg ctt cac aaa aag gaa gat gga att tgg 2975 Leu Ser His Ser Leu Leu Leu Leu His Lys Lys Glu Asp Gly Ile Trp 100 105 110 tcc act gat att tta aag gac cag aaa gaa ccc aaa aat aag acc ttt 3023 Ser Thr Asp Ile Leu Lys Asp Gln Lys Glu Pro Lys Asn Lys Thr Phe 115 120 125 cta aga tgc gag gcc aag aat tat tct gga cgt ttc acc tgc tgg tgg 3071 Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly Arg Phe Thr Cys Trp Trp 130 135 140 ctg acg aca atc agt act gat ttg aca ttc agt gtc aaa agc agc aga 3119 Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe Ser Val Lys Ser Ser Arg 145 150 155 160 ggc tct tct gac ccc caa ggg gtg acg tgc gga gct gct aca ctc tct 3167 Gly Ser Ser Asp Pro Gln Gly Val Thr Cys Gly Ala Ala Thr Leu Ser 165 170 175 gca gag aga gtc aga ggg gac aac aag gag tat gag tac tca gtg gag 3215 Ala Glu Arg Val Arg Gly Asp Asn Lys Glu Tyr Glu Tyr Ser Val Glu 180 185 190 tgc cag gag gac agt gcc tgc cca gct gct gag gag agt ctg ccc att 3263 Cys Gln Glu Asp Ser Ala Cys Pro Ala Ala Glu Glu Ser Leu Pro Ile 195 200 205 gag gtc atg gtg gat gcc gtt cac aag ctc aag tat gaa aac tac acc 3311 Glu Val Met Val Asp Ala Val His Lys Leu Lys Tyr Glu Asn Tyr Thr 210 215 220 agc agc ttc ttc atc agg gac atc atc aaa cct gac cca ccc aac aac 3359 Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys Pro Asp Pro Pro Asn Asn 225 230 235 240 ttg cag ctg aag cca tta aag aat tct cgg cag gtg gag gtc agc tgg 3407 Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg Gln Val Glu Val Ser Trp 245 250 255 gag tac cct gac acc tgg agt act cca cat tcc tac ttc tcc ctg aca 3455 Glu Tyr Pro Asp Thr Trp Ser Thr Pro His Ser Tyr Phe Ser Leu Thr 260 265 270 ttc tgc gtt cag gtc cag ggc aag agc aag aga gaa aag aaa gat aga 3503 Phe Cys Val Gln Val Gln Gly Lys Ser Lys Arg Glu Lys Lys Asp Arg 275 280 285 gtc ttc acc gac aag acc tca gcc acg gtc atc tgc cgc aaa aat gcc 3551 Val Phe Thr Asp Lys Thr Ser Ala Thr Val Ile Cys Arg Lys Asn Ala 290 295 300 agc att agc gtg cgg gcc cag gac cgc tac tat agc tca tct tgg agc 3599 Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr Tyr Ser Ser Ser Trp Ser 305 310 315 320 gaa tgg gca tct gtg ccc tgc agt ggt ggc ggt gga agc ggt ggc ggt 3647 Glu Trp Ala Ser Val Pro Cys Ser Gly Gly Gly Gly Ser Gly Gly Gly 325 330 335 gga agc ggt ggc ggt gga agc cca tgg aga aac ctc ccc gtg gcc act 3695 Gly Ser Gly Gly Gly Gly Ser Pro Trp Arg Asn Leu Pro Val Ala Thr 340 345 350 cca gac cca gga atg ttc cca tgc ctt cac cac tcc caa aac ctg ctg 3743 Pro Asp Pro Gly Met Phe Pro Cys Leu His His Ser Gln Asn Leu Leu 355 360 365 agg gcc gtc agc aac atg ctc cag aag gcc aga caa act cta gaa ttt 3791 Arg Ala Val Ser Asn Met Leu Gln Lys Ala Arg Gln Thr Leu Glu Phe 370 375 380 tac cct tgc act tct gaa gag att gat cat gaa gat atc aca aaa gat 3839 Tyr Pro Cys Thr Ser Glu Glu Ile Asp His Glu Asp Ile Thr Lys Asp 385 390 395 400 aaa acc agc aca gtg gag gcc tgt tta cca ttg gaa tta acc aag aat 3887 Lys Thr Ser Thr Val Glu Ala Cys Leu Pro Leu Glu Leu Thr Lys Asn 405 410 415 gag agt tgc cta aat tcc aga gag acc tct ttc ata act aat ggg agt 3935 Glu Ser Cys Leu Asn Ser Arg Glu Thr Ser Phe Ile Thr Asn Gly Ser 420 425 430 tgc ctg gcc tcc aga aag acc tct ttt atg atg gcc ctg tgc ctt agt 3983 Cys Leu Ala Ser Arg Lys Thr Ser Phe Met Met Ala Leu Cys Leu Ser 435 440 445 agt att tat gaa gac ttg aag atg tac cag gtg gag ttc aag acc atg 4031 Ser Ile Tyr Glu Asp Leu Lys Met Tyr Gln Val Glu Phe Lys Thr Met 450 455 460 aat gca aag ctt ctg atg gat cct aag agg cag atc ttt cta gat caa 4079 Asn Ala Lys Leu Leu Met Asp Pro Lys Arg Gln Ile Phe Leu Asp Gln 465 470 475 480 aac atg ctg gca gtt att gat gag ctg atg cag gcc ctg aat ttc aac 4127 Asn Met Leu Ala Val Ile Asp Glu Leu Met Gln Ala Leu Asn Phe Asn 485 490 495 agt gag act gtg cca caa aaa tcc tcc ctt gaa gaa ccg gat ttt tat 4175 Ser Glu Thr Val Pro Gln Lys Ser Ser Leu Glu Glu Pro Asp Phe Tyr 500 505 510 aaa act aaa atc aag ctc tgc ata ctt ctt cat gct ttc aga att cgg 4223 Lys Thr Lys Ile Lys Leu Cys Ile Leu Leu His Ala Phe Arg Ile Arg 515 520 525 gca gtg act att gat aga gtg atg agc tat ctg aat gct tcc taa 4268 Ala Val Thr Ile Asp Arg Val Met Ser Tyr Leu Asn Ala Ser 530 535 540 aaagcgaggt gcggccgctt ccctttagtg agggttaatg cttcgagcag acatgataag 4328 atacattgat gagtttggac aaaccacaac tagaatgcag tgaaaaaaat gctttatttg 4388 tgaaatttgt gatgctattg ctttatttgt aaccattata agctgcaata aacaagttaa 4448 caacaacaat tgcattcatt ttatgtttca ggttcagggg gagatgtggg aggtttttta 4508 aagcaagtaa aacctctaca aatgtggtaa aatccgataa ggatcgatcc gggctggcgt 4568 aatagcgaag aggcccgcac cgatcgccct tcccaacagt tgcgcagcct gaatggcgaa 4628 tggacgcgcc ctgtagcggc gcattaagcg cggcgggtgt ggtggttacg cgcagcgtga 4688 ccgctacact tgccagcgcc ctagcgcccg ctcctttcgc tttcttccct tcctttctcg 4748 ccacgttcgc cggctttccc cgtcaagctc taaatcgggg gctcccttta gggttccgat 4808 ttagagcttt acggcacctc gaccgcaaaa aacttgattt gggtgatggt tcacgtagtg 4868 ggccatcgcc ctgatagacg gtttttcgcc ctttgacgtt ggagtccacg ttctttaata 4928 gtggactctt gttccaaact ggaacaacac tcaaccctat ctcggtctat tcttttgatt 4988 tataagggat tttgccgatt tcggcctatt ggttaaaaaa tgagctgatt taacaaatat 5048 ttaacgcgaa ttttaacaaa atattaacgt ttacaatttc gcctgatgcg gtattttctc 5108 cttacgcatc tgtgcggtat ttcacaccgc atacgcggat ctgcgcagca ccatggcctg 5168 aaataacctc tgaaagagga acttggttag gtaccttctg aggcggaaag aaccagctgt 5228 ggaatgtgtg tcagttaggg tgtggaaagt ccccaggctc cccagcaggc agaagtatgc 5288 aaagcatgca tctcaattag tcagcaacca ggtgtggaaa gtccccaggc tccccagcag 5348 gcagaagtat gcaaagcatg catctcaatt agtcagcaac catagtcccg cccctaactc 5408 cgcccatccc gcccctaact ccgcccagtt ccgcccattc tccgccccat ggctgactaa 5468 ttttttttat ttatgcagag gccgaggccg cctcggcctc tgagctattc cagaagtagt 5528 gaggaggctt ttttggaggc ctaggctttt gcaaaaagct tgattcttct gacacaacag 5588 tctcgaactt aaggctagag ccaccatgat tgaacaagat ggattgcacg caggttctcc 5648 ggccgcttgg gtggagaggc tattcggcta tgactgggca caacagacaa tcggctgctc 5708 tgatgccgcc gtgttccggc tgtcagcgca ggggcgcccg gttctttttg tcaagaccga 5768 cctgtccggt gccctgaatg aactgcagga cgaggcagcg cggctatcgt ggctggccac 5828 gacgggcgtt ccttgcgcag ctgtgctcga cgttgtcact gaagcgggaa gggactggct 5888 gctattgggc gaagtgccgg ggcaggatct cctgtcatct caccttgctc ctgccgagaa 5948 agtatccatc atggctgatg caatgcggcg gctgcatacg cttgatccgg ctacctgccc 6008 attcgaccac caagcgaaac atcgcatcga gcgagcacgt actcggatgg aagccggtct 6068 tgtcgatcag gatgatctgg acgaagagca tcaggggctc gcgccagccg aactgttcgc 6128 caggctcaag gcgcgcatgc ccgacggcga ggatctcgtc gtgacccatg gcgatgcctg 6188 cttgccgaat atcatggtgg aaaatggccg cttttctgga ttcatcgact gtggccggct 6248 gggtgtggcg gaccgctatc aggacatagc gttggctacc cgtgatattg ctgaagagct 6308 tggcggcgaa tgggctgacc gcttcctcgt gctttacggt atcgccgctc ccgattcgca 6368 gcgcatcgcc ttctatcgcc ttcttgacga gttcttctga gcgggactct ggggttcgaa 6428 atgaccgacc aagcgacgcc caacctgcca tcacgatggc cgcaataaaa tatctttatt 6488 ttcattacat ctgtgtgttg gttttttgtg tgaatcgata gcgataagga tccgcgtatg 6548 gtgcactctc agtacaatct gctctgatgc cgcatagtta agccagcccc gacacccgcc 6608 aacacccgct gacgcgccct gacgggcttg tctgctcccg gcatccgctt acagacaagc 6668 tgtgaccgtc tccgggagct gcatgtgtca gaggttttca ccgtcatcac cgaaacgcgc 6728 gagacgaaag ggcctcgtga tacgcctatt tttataggtt aatgtcatga taataatggt 6788 ttcttagacg tcaggtggca cttttcgggg aaatgtgcgc ggaaccccta tttgtttatt 6848 tttctaaata cattcaaata tgtatccgct catgagacaa taaccctgat aaatgcttca 6908 ataatattga aaaaggaaga gtatgagtat tcaacatttc cgtgtcgccc ttattccctt 6968 ttttgcggca ttttgccttc ctgtttttgc tcacccagaa acgctggtga aagtaaaaga 7028 tgctgaagat cagttgggtg cacgagtggg ttacatcgaa ctggatctca acagcggtaa 7088 gatccttgag agttttcgcc ccgaagaacg ttttccaatg atgagcactt ttaaagttct 7148 gctatgtggc gcggtattat cccgtattga cgccgggcaa gagcaactcg gtcgccgcat 7208 acactattct cagaatgact tggttgagta ctcaccagtc acagaaaagc atcttacgga 7268 tggcatgaca gtaagagaat tatgcagtgc tgccataacc atgagtgata acactgcggc 7328 caacttactt ctgacaacga tcggaggacc gaaggagcta accgcttttt tgcacaacat 7388 gggggatcat gtaactcgcc ttgatcgttg ggaaccggag ctgaatgaag ccataccaaa 7448 cgacgagcgt gacaccacga tgcctgtagc aatggcaaca acgttgcgca aactattaac 7508 tggcgaacta cttactctag cttcccggca acaattaata gactggatgg aggcggataa 7568 agttgcagga ccacttctgc gctcggccct tccggctggc tggtttattg ctgataaatc 7628 tggagccggt gagcgtgggt ctcgcggtat cattgcagca ctggggccag atggtaagcc 7688 ctcccgtatc gtagttatct acacgacggg gagtcaggca actatggatg aacgaaatag 7748 acagatcgct gagataggtg cctcactgat taagcattgg taactgtcag accaagttta 7808 ctcatatata ctttagattg atttaaaact tcatttttaa tttaaaagga tctaggtgaa 7868 gatccttttt gataatctca tgaccaaaat cccttaacgt gagttttcgt tccactgagc 7928 gtcagacccc gtagaaaaga tcaaaggatc ttcttgagat cctttttttc tgcgcgtaat 7988 ctgctgcttg caaacaaaaa aaccaccgct accagcggtg gtttgtttgc cggatcaaga 8048 gctaccaact ctttttccga aggtaactgg cttcagcaga gcgcagatac caaatactgt 8108 ccttctagtg tagccgtagt taggccacca cttcaagaac tctgtagcac cgcctacata 8168 cctcgctctg ctaatcctgt taccagtggc tgctgccagt ggcgataagt cgtgtcttac 8228 cgggttggac tcaagacgat agttaccgga taaggcgcag cggtcgggct gaacgggggg 8288 ttcgtgcaca cagcccagct tggagcgaac gacctacacc gaactgagat acctacagcg 8348 tgagctatga gaaagcgcca cgcttcccga agggagaaag gcggacaggt atccggtaag 8408 cggcagggtc ggaacaggag agcgcacgag ggagcttcca gggggaaacg cctggtatct 8468 ttatagtcct gtcgggtttc gccacctctg acttgagcgt cgatttttgt gatgctcgtc 8528 aggggggcgg agcctatgga aaaacgccag caacgcggcc tttttacggt tcctggcctt 8588 ttgctggcct tttgctcaca tggctcgaca gatct 8623 6 542 PRT Artificial Sequence Description of Artificial Sequence plasmid 6 Met Cys His Gln Gln Leu Val Ile Ser Trp Phe Ser Leu Val Phe Leu 1 5 10 15 Ala Ser Pro Leu Val Ala Ile Trp Glu Leu Lys Lys Asp Val Tyr Val 20 25 30 Val Glu Leu Asp Trp Tyr Pro Asp Ala Pro Gly Glu Met Val Val Leu 35 40 45 Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile Thr Trp Thr Leu Asp Gln 50 55 60 Ser Ser Glu Val Leu Gly Ser Gly Lys Thr Leu Thr Ile Gln Val Lys 65 70 75 80 Glu Phe Gly Asp Ala Gly Gln Tyr Thr Cys His Lys Gly Gly Glu Val 85 90 95 Leu Ser His Ser Leu Leu Leu Leu His Lys Lys Glu Asp Gly Ile Trp 100 105 110 Ser Thr Asp Ile Leu Lys Asp Gln Lys Glu Pro Lys Asn Lys Thr Phe 115 120 125 Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly Arg Phe Thr Cys Trp Trp 130 135 140 Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe Ser Val Lys Ser Ser Arg 145 150 155 160 Gly Ser Ser Asp Pro Gln Gly Val Thr Cys Gly Ala Ala Thr Leu Ser 165 170 175 Ala Glu Arg Val Arg Gly Asp Asn Lys Glu Tyr Glu Tyr Ser Val Glu 180 185 190 Cys Gln Glu Asp Ser Ala Cys Pro Ala Ala Glu Glu Ser Leu Pro Ile 195 200 205 Glu Val Met Val Asp Ala Val His Lys Leu Lys Tyr Glu Asn Tyr Thr 210 215 220 Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys Pro Asp Pro Pro Asn Asn 225 230 235 240 Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg Gln Val Glu Val Ser Trp 245 250 255 Glu Tyr Pro Asp Thr Trp Ser Thr Pro His Ser Tyr Phe Ser Leu Thr 260 265 270 Phe Cys Val Gln Val Gln Gly Lys Ser Lys Arg Glu Lys Lys Asp Arg 275 280 285 Val Phe Thr Asp Lys Thr Ser Ala Thr Val Ile Cys Arg Lys Asn Ala 290 295 300 Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr Tyr Ser Ser Ser Trp Ser 305 310 315 320 Glu Trp Ala Ser Val Pro Cys Ser Gly Gly Gly Gly Ser Gly Gly Gly 325 330 335 Gly Ser Gly Gly Gly Gly Ser Pro Trp Arg Asn Leu Pro Val Ala Thr 340 345 350 Pro Asp Pro Gly Met Phe Pro Cys Leu His His Ser Gln Asn Leu Leu 355 360 365 Arg Ala Val Ser Asn Met Leu Gln Lys Ala Arg Gln Thr Leu Glu Phe 370 375 380 Tyr Pro Cys Thr Ser Glu Glu Ile Asp His Glu Asp Ile Thr Lys Asp 385 390 395 400 Lys Thr Ser Thr Val Glu Ala Cys Leu Pro Leu Glu Leu Thr Lys Asn 405 410 415 Glu Ser Cys Leu Asn Ser Arg Glu Thr Ser Phe Ile Thr Asn Gly Ser 420 425 430 Cys Leu Ala Ser Arg Lys Thr Ser Phe Met Met Ala Leu Cys Leu Ser 435 440 445 Ser Ile Tyr Glu Asp Leu Lys Met Tyr Gln Val Glu Phe Lys Thr Met 450 455 460 Asn Ala Lys Leu Leu Met Asp Pro Lys Arg Gln Ile Phe Leu Asp Gln 465 470 475 480 Asn Met Leu Ala Val Ile Asp Glu Leu Met Gln Ala Leu Asn Phe Asn 485 490 495 Ser Glu Thr Val Pro Gln Lys Ser Ser Leu Glu Glu Pro Asp Phe Tyr 500 505 510 Lys Thr Lys Ile Lys Leu Cys Ile Leu Leu His Ala Phe Arg Ile Arg 515 520 525 Ala Val Thr Ile Asp Arg Val Met Ser Tyr Leu Asn Ala Ser 530 535 540 7 8608 DNA Artificial Sequence Description of Artificial Sequence plasmid 7 tcaatattgg ccattagcca tattattcat tggttatata gcataaatca atattggcta 60 ttggccattg catacgttgt atctatatca taatatgtac atttatattg gctcatgtcc 120 aatatgaccg ccatgttggc attgattatt gactagttat taatagtaat caattacggg 180 gtcattagtt catagcccat atatggagtt ccgcgttaca taacttacgg taaatggccc 240 gcctggctga ccgcccaacg acccccgccc attgacgtca ataatgacgt atgttcccat 300 agtaacgcca atagggactt tccattgacg tcaatgggtg gagtatttac ggtaaactgc 360 ccacttggca gtacatcaag tgtatcatat gccaagtccg ccccctattg acgtcaatga 420 cggtaaatgg cccgcctggc attatgccca gtacatgacc ttacgggact ttcctacttg 480 gcagtacatc tacgtattag tcatcgctat taccatggtg atgcggtttt ggcagtacac 540 caatgggcgt ggatagcggt ttgactcacg gggatttcca agtctccacc ccattgacgt 600 caatgggagt ttgttttggc accaaaatca acgggacttt ccaaaatgtc gtaacaactg 660 cgatcgcccg ccccgttgac gcaaatgggc ggtaggcgtg tacggtggga ggtctatata 720 agcagagctc gtttagtgaa ccgtcagatc actagaagct ttattgcggt agtttatcac 780 agttaaattg ctaacgcagt cagtgcttct gacacaacag tctcgaactt aagctgcagt 840 gactctctta aggtagcctt gcagaagttg gtcgtgaggc actgggcagg taagtatcaa 900 ggttacaaga caggtttaag gagaccaata gaaactgggc ttgtcgagac agagaagact 960 cttgcgtttc tgataggcac ctattggtct tactgacatc cactttgcct ttctctccac 1020 aggtgtccac tcccagttca attacagctc ttaaggctag agtacttaat acgactcact 1080 ataggctaga tgggccacac acggaggcag ggaacatcac catccaagtg tccatacctc 1140 aatttctttc agctcttggt gctggctggt ctttctcact tctgttcagg tgttatccac 1200 gtgaccaagg aagtgaaaga agtggcaacg ctgtcctgtg gtcacaatgt ttctgttgaa 1260 gagctggcac aaactcgcat ctactggcaa aaggagaaga aaatggtgct gactatgatg 1320 tctggggaca tgaatatatg gcccgagtac aagaaccgga ccatctttga tatcactaat 1380 aacctctcca ttgtgatcct ggctctgcgc ccatctgacg agggcacata cgagtgtgtt 1440 gttctgaagt atgaaaaaga cgctttcaag cgggaacacc tggctgaagt gacgttatca 1500 gtcaaagctg acttccctac acctagtata tctgactttg aaattccaac ttctaatatt 1560 agaaggataa tttgctcaac ctctggaggt tttccagagc ctcacctctc ctggttggaa 1620 aatggagaag aattaaatgc catcaacaca acagtttccc aagatcctga aactgagctc 1680 tatgctgtta gcagcaaact ggatttcaat atgacaacca accacagctt catgtgtctc 1740 atcaagtatg gacatttaag agtgaatcag accttcaact ggaatacaac caagcaagag 1800 cattttcctg ataacctgct cccatcctgg gccattacct taatctcagt aaatggaatt 1860 tttgtgatat gctgcctgac ctactgcttt gccccaagat gcagagagag aaggaggaat 1920 gagagattga gaagggaaag tgtacgccct gtataacagt gtccgcagaa gcaaggggct 1980 gaaaacgcgt cgagcatgca tctagggcgg ccaattccgc ccctctccct cccccccccc 2040 taacgttact ggccgaagcc gcttggaata aggccggtgt gcgtttgtct atatgtgatt 2100 ttccaccata ttgccgtctt ttggcaatgt gagggcccgg aaacctggcc ctgtcttctt 2160 gacgagcatt cctaggggtc tttcccctct cgccaaagga atgcaaggtc tgttgaatgt 2220 cgtgaaggaa gcagttcctc tggaagcttc ttgaagacaa acaacgtctg tagcgaccct 2280 ttgcaggcag cggaaccccc cacctggcga caggtgcctc tgcggccaaa agccacgtgt 2340 ataagataca cctgcaaagg cggcacaacc ccagtgccac gttgtgagtt ggatagttgt 2400 ggaaagagtc aaatggctct cctcaagcgt attcaacaag gggctgaagg atgcccagaa 2460 ggtaccccat tgtatgggat ctgatctggg gcctcggtgc acatgcttta catgtgttta 2520 gtcgaggtta aaaaaacgtc taggcccccc gaaccacggg gacgtggttt tcctttgaaa 2580 aacacgatga taagcttgcc acaacccggg atcctctaga gtcgacggcc cagagcaag 2639 atg tgt cac cag cag ttg gtc atc tct tgg ttt tcc ctg gtt ttt ctg 2687 Met Cys His Gln Gln Leu Val Ile Ser Trp Phe Ser Leu Val Phe Leu 1 5 10 15 gca tct ccc ctc gtg gcc ata tgg gaa ctg aag aaa gat gtt tat gtc 2735 Ala Ser Pro Leu Val Ala Ile Trp Glu Leu Lys Lys Asp Val Tyr Val 20 25 30 gta gaa ttg gat tgg tat ccg gat gcc cct gga gaa atg gtg gtc ctc 2783 Val Glu Leu Asp Trp Tyr Pro Asp Ala Pro Gly Glu Met Val Val Leu 35 40 45 acc tgt gac acc cct gaa gaa gat ggt atc acc tgg acc ttg gac cag 2831 Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile Thr Trp Thr Leu Asp Gln 50 55 60 agc agt gag gtc tta ggc tct ggc aaa acc ctg acc atc caa gtc aaa 2879 Ser Ser Glu Val Leu Gly Ser Gly Lys Thr Leu Thr Ile Gln Val Lys 65 70 75 80 gag ttt gga gat gct ggc cag tac acc tgt cac aaa gga ggc gag gtt 2927 Glu Phe Gly Asp Ala Gly Gln Tyr Thr Cys His Lys Gly Gly Glu Val 85 90 95 cta agc cat tcg ctc ctg ctg ctt cac aaa aag gaa gat gga att tgg 2975 Leu Ser His Ser Leu Leu Leu Leu His Lys Lys Glu Asp Gly Ile Trp 100 105 110 tcc act gat att tta aag gac cag aaa gaa ccc aaa aat aag acc ttt 3023 Ser Thr Asp Ile Leu Lys Asp Gln Lys Glu Pro Lys Asn Lys Thr Phe 115 120 125 cta aga tgc gag gcc aag aat tat tct gga cgt ttc acc tgc tgg tgg 3071 Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly Arg Phe Thr Cys Trp Trp 130 135 140 ctg acg aca atc agt act gat ttg aca ttc agt gtc aaa agc agc aga 3119 Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe Ser Val Lys Ser Ser Arg 145 150 155 160 ggc tct tct gac ccc caa ggg gtg acg tgc gga gct gct aca ctc tct 3167 Gly Ser Ser Asp Pro Gln Gly Val Thr Cys Gly Ala Ala Thr Leu Ser 165 170 175 gca gag aga gtc aga ggg gac aac aag gag tat gag tac tca gtg gag 3215 Ala Glu Arg Val Arg Gly Asp Asn Lys Glu Tyr Glu Tyr Ser Val Glu 180 185 190 tgc cag gag gac agt gcc tgc cca gct gct gag gag agt ctg ccc att 3263 Cys Gln Glu Asp Ser Ala Cys Pro Ala Ala Glu Glu Ser Leu Pro Ile 195 200 205 gag gtc atg gtg gat gcc gtt cac aag ctc aag tat gaa aac tac acc 3311 Glu Val Met Val Asp Ala Val His Lys Leu Lys Tyr Glu Asn Tyr Thr 210 215 220 agc agc ttc ttc atc agg gac atc atc aaa cct gac cca ccc aac aac 3359 Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys Pro Asp Pro Pro Asn Asn 225 230 235 240 ttg cag ctg aag cca tta aag aat tct cgg cag gtg gag gtc agc tgg 3407 Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg Gln Val Glu Val Ser Trp 245 250 255 gag tac cct gac acc tgg agt act cca cat tcc tac ttc tcc ctg aca 3455 Glu Tyr Pro Asp Thr Trp Ser Thr Pro His Ser Tyr Phe Ser Leu Thr 260 265 270 ttc tgc gtt cag gtc cag ggc aag agc aag aga gaa aag aaa gat aga 3503 Phe Cys Val Gln Val Gln Gly Lys Ser Lys Arg Glu Lys Lys Asp Arg 275 280 285 gtc ttc acc gac aag acc tca gcc acg gtc atc tgc cgc aaa aat gcc 3551 Val Phe Thr Asp Lys Thr Ser Ala Thr Val Ile Cys Arg Lys Asn Ala 290 295 300 agc att agc gtg cgg gcc cag gac cgc tac tat agc tca tct tgg agc 3599 Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr Tyr Ser Ser Ser Trp Ser 305 310 315 320 gaa tgg gca tct gtg ccc tgc agt ggt ggc ggt gga agc ggt ggc ggt 3647 Glu Trp Ala Ser Val Pro Cys Ser Gly Gly Gly Gly Ser Gly Gly Gly 325 330 335 gga agc cca tgg aga aac ctc ccc gtg gcc act cca gac cca gga atg 3695 Gly Ser Pro Trp Arg Asn Leu Pro Val Ala Thr Pro Asp Pro Gly Met 340 345 350 ttc cca tgc ctt cac cac tcc caa aac ctg ctg agg gcc gtc agc aac 3743 Phe Pro Cys Leu His His Ser Gln Asn Leu Leu Arg Ala Val Ser Asn 355 360 365 atg ctc cag aag gcc aga caa act cta gaa ttt tac cct tgc act tct 3791 Met Leu Gln Lys Ala Arg Gln Thr Leu Glu Phe Tyr Pro Cys Thr Ser 370 375 380 gaa gag att gat cat gaa gat atc aca aaa gat aaa acc agc aca gtg 3839 Glu Glu Ile Asp His Glu Asp Ile Thr Lys Asp Lys Thr Ser Thr Val 385 390 395 400 gag gcc tgt tta cca ttg gaa tta acc aag aat gag agt tgc cta aat 3887 Glu Ala Cys Leu Pro Leu Glu Leu Thr Lys Asn Glu Ser Cys Leu Asn 405 410 415 tcc aga gag acc tct ttc ata act aat ggg agt tgc ctg gcc tcc aga 3935 Ser Arg Glu Thr Ser Phe Ile Thr Asn Gly Ser Cys Leu Ala Ser Arg 420 425 430 aag acc tct ttt atg atg gcc ctg tgc ctt agt agt att tat gaa gac 3983 Lys Thr Ser Phe Met Met Ala Leu Cys Leu Ser Ser Ile Tyr Glu Asp 435 440 445 ttg aag atg tac cag gtg gag ttc aag acc atg aat gca aag ctt ctg 4031 Leu Lys Met Tyr Gln Val Glu Phe Lys Thr Met Asn Ala Lys Leu Leu 450 455 460 atg gat cct aag agg cag atc ttt cta gat caa aac atg ctg gca gtt 4079 Met Asp Pro Lys Arg Gln Ile Phe Leu Asp Gln Asn Met Leu Ala Val 465 470 475 480 att gat gag ctg atg cag gcc ctg aat ttc aac agt gag act gtg cca 4127 Ile Asp Glu Leu Met Gln Ala Leu Asn Phe Asn Ser Glu Thr Val Pro 485 490 495 caa aaa tcc tcc ctt gaa gaa ccg gat ttt tat aaa act aaa atc aag 4175 Gln Lys Ser Ser Leu Glu Glu Pro Asp Phe Tyr Lys Thr Lys Ile Lys 500 505 510 ctc tgc ata ctt ctt cat gct ttc aga att cgg gca gtg act att gat 4223 Leu Cys Ile Leu Leu His Ala Phe Arg Ile Arg Ala Val Thr Ile Asp 515 520 525 aga gtg atg agc tat ctg aat gct tcc taa aaagcgaggt gcggccgctt 4273 Arg Val Met Ser Tyr Leu Asn Ala Ser 530 535 ccctttagtg agggttaatg cttcgagcag acatgataag atacattgat gagtttggac 4333 aaaccacaac tagaatgcag tgaaaaaaat gctttatttg tgaaatttgt gatgctattg 4393 ctttatttgt aaccattata agctgcaata aacaagttaa caacaacaat tgcattcatt 4453 ttatgtttca ggttcagggg gagatgtggg aggtttttta aagcaagtaa aacctctaca 4513 aatgtggtaa aatccgataa ggatcgatcc gggctggcgt aatagcgaag aggcccgcac 4573 cgatcgccct tcccaacagt tgcgcagcct gaatggcgaa tggacgcgcc ctgtagcggc 4633 gcattaagcg cggcgggtgt ggtggttacg cgcagcgtga ccgctacact tgccagcgcc 4693 ctagcgcccg ctcctttcgc tttcttccct tcctttctcg ccacgttcgc cggctttccc 4753 cgtcaagctc taaatcgggg gctcccttta gggttccgat ttagagcttt acggcacctc 4813 gaccgcaaaa aacttgattt gggtgatggt tcacgtagtg ggccatcgcc ctgatagacg 4873 gtttttcgcc ctttgacgtt ggagtccacg ttctttaata gtggactctt gttccaaact 4933 ggaacaacac tcaaccctat ctcggtctat tcttttgatt tataagggat tttgccgatt 4993 tcggcctatt ggttaaaaaa tgagctgatt taacaaatat ttaacgcgaa ttttaacaaa 5053 atattaacgt ttacaatttc gcctgatgcg gtattttctc cttacgcatc tgtgcggtat 5113 ttcacaccgc atacgcggat ctgcgcagca ccatggcctg aaataacctc tgaaagagga 5173 acttggttag gtaccttctg aggcggaaag aaccagctgt ggaatgtgtg tcagttaggg 5233 tgtggaaagt ccccaggctc cccagcaggc agaagtatgc aaagcatgca tctcaattag 5293 tcagcaacca ggtgtggaaa gtccccaggc tccccagcag gcagaagtat gcaaagcatg 5353 catctcaatt agtcagcaac catagtcccg cccctaactc cgcccatccc gcccctaact 5413 ccgcccagtt ccgcccattc tccgccccat ggctgactaa ttttttttat ttatgcagag 5473 gccgaggccg cctcggcctc tgagctattc cagaagtagt gaggaggctt ttttggaggc 5533 ctaggctttt gcaaaaagct tgattcttct gacacaacag tctcgaactt aaggctagag 5593 ccaccatgat tgaacaagat ggattgcacg caggttctcc ggccgcttgg gtggagaggc 5653 tattcggcta tgactgggca caacagacaa tcggctgctc tgatgccgcc gtgttccggc 5713 tgtcagcgca ggggcgcccg gttctttttg tcaagaccga cctgtccggt gccctgaatg 5773 aactgcagga cgaggcagcg cggctatcgt ggctggccac gacgggcgtt ccttgcgcag 5833 ctgtgctcga cgttgtcact gaagcgggaa gggactggct gctattgggc gaagtgccgg 5893 ggcaggatct cctgtcatct caccttgctc ctgccgagaa agtatccatc atggctgatg 5953 caatgcggcg gctgcatacg cttgatccgg ctacctgccc attcgaccac caagcgaaac 6013 atcgcatcga gcgagcacgt actcggatgg aagccggtct tgtcgatcag gatgatctgg 6073 acgaagagca tcaggggctc gcgccagccg aactgttcgc caggctcaag gcgcgcatgc 6133 ccgacggcga ggatctcgtc gtgacccatg gcgatgcctg cttgccgaat atcatggtgg 6193 aaaatggccg cttttctgga ttcatcgact gtggccggct gggtgtggcg gaccgctatc 6253 aggacatagc gttggctacc cgtgatattg ctgaagagct tggcggcgaa tgggctgacc 6313 gcttcctcgt gctttacggt atcgccgctc ccgattcgca gcgcatcgcc ttctatcgcc 6373 ttcttgacga gttcttctga gcgggactct ggggttcgaa atgaccgacc aagcgacgcc 6433 caacctgcca tcacgatggc cgcaataaaa tatctttatt ttcattacat ctgtgtgttg 6493 gttttttgtg tgaatcgata gcgataagga tccgcgtatg gtgcactctc agtacaatct 6553 gctctgatgc cgcatagtta agccagcccc gacacccgcc aacacccgct gacgcgccct 6613 gacgggcttg tctgctcccg gcatccgctt acagacaagc tgtgaccgtc tccgggagct 6673 gcatgtgtca gaggttttca ccgtcatcac cgaaacgcgc gagacgaaag ggcctcgtga 6733 tacgcctatt tttataggtt aatgtcatga taataatggt ttcttagacg tcaggtggca 6793 cttttcgggg aaatgtgcgc ggaaccccta tttgtttatt tttctaaata cattcaaata 6853 tgtatccgct catgagacaa taaccctgat aaatgcttca ataatattga aaaaggaaga 6913 gtatgagtat tcaacatttc cgtgtcgccc ttattccctt ttttgcggca ttttgccttc 6973 ctgtttttgc tcacccagaa acgctggtga aagtaaaaga tgctgaagat cagttgggtg 7033 cacgagtggg ttacatcgaa ctggatctca acagcggtaa gatccttgag agttttcgcc 7093 ccgaagaacg ttttccaatg atgagcactt ttaaagttct gctatgtggc gcggtattat 7153 cccgtattga cgccgggcaa gagcaactcg gtcgccgcat acactattct cagaatgact 7213 tggttgagta ctcaccagtc acagaaaagc atcttacgga tggcatgaca gtaagagaat 7273 tatgcagtgc tgccataacc atgagtgata acactgcggc caacttactt ctgacaacga 7333 tcggaggacc gaaggagcta accgcttttt tgcacaacat gggggatcat gtaactcgcc 7393 ttgatcgttg ggaaccggag ctgaatgaag ccataccaaa cgacgagcgt gacaccacga 7453 tgcctgtagc aatggcaaca acgttgcgca aactattaac tggcgaacta cttactctag 7513 cttcccggca acaattaata gactggatgg aggcggataa agttgcagga ccacttctgc 7573 gctcggccct tccggctggc tggtttattg ctgataaatc tggagccggt gagcgtgggt 7633 ctcgcggtat cattgcagca ctggggccag atggtaagcc ctcccgtatc gtagttatct 7693 acacgacggg gagtcaggca actatggatg aacgaaatag acagatcgct gagataggtg 7753 cctcactgat taagcattgg taactgtcag accaagttta ctcatatata ctttagattg 7813 atttaaaact tcatttttaa tttaaaagga tctaggtgaa gatccttttt gataatctca 7873 tgaccaaaat cccttaacgt gagttttcgt tccactgagc gtcagacccc gtagaaaaga 7933 tcaaaggatc ttcttgagat cctttttttc tgcgcgtaat ctgctgcttg caaacaaaaa 7993 aaccaccgct accagcggtg gtttgtttgc cggatcaaga gctaccaact ctttttccga 8053 aggtaactgg cttcagcaga gcgcagatac caaatactgt ccttctagtg tagccgtagt 8113 taggccacca cttcaagaac tctgtagcac cgcctacata cctcgctctg ctaatcctgt 8173 taccagtggc tgctgccagt ggcgataagt cgtgtcttac cgggttggac tcaagacgat 8233 agttaccgga taaggcgcag cggtcgggct gaacgggggg ttcgtgcaca cagcccagct 8293 tggagcgaac gacctacacc gaactgagat acctacagcg tgagctatga gaaagcgcca 8353 cgcttcccga agggagaaag gcggacaggt atccggtaag cggcagggtc ggaacaggag 8413 agcgcacgag ggagcttcca gggggaaacg cctggtatct ttatagtcct gtcgggtttc 8473 gccacctctg acttgagcgt cgatttttgt gatgctcgtc aggggggcgg agcctatgga 8533 aaaacgccag caacgcggcc tttttacggt tcctggcctt ttgctggcct tttgctcaca 8593 tggctcgaca gatct 8608 8 537 PRT Artificial Sequence Description of Artificial Sequence plasmid 8 Met Cys His Gln Gln Leu Val Ile Ser Trp Phe Ser Leu Val Phe Leu 1 5 10 15 Ala Ser Pro Leu Val Ala Ile Trp Glu Leu Lys Lys Asp Val Tyr Val 20 25 30 Val Glu Leu Asp Trp Tyr Pro Asp Ala Pro Gly Glu Met Val Val Leu 35 40 45 Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile Thr Trp Thr Leu Asp Gln 50 55 60 Ser Ser Glu Val Leu Gly Ser Gly Lys Thr Leu Thr Ile Gln Val Lys 65 70 75 80 Glu Phe Gly Asp Ala Gly Gln Tyr Thr Cys His Lys Gly Gly Glu Val 85 90 95 Leu Ser His Ser Leu Leu Leu Leu His Lys Lys Glu Asp Gly Ile Trp 100 105 110 Ser Thr Asp Ile Leu Lys Asp Gln Lys Glu Pro Lys Asn Lys Thr Phe 115 120 125 Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly Arg Phe Thr Cys Trp Trp 130 135 140 Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe Ser Val Lys Ser Ser Arg 145 150 155 160 Gly Ser Ser Asp Pro Gln Gly Val Thr Cys Gly Ala Ala Thr Leu Ser 165 170 175 Ala Glu Arg Val Arg Gly Asp Asn Lys Glu Tyr Glu Tyr Ser Val Glu 180 185 190 Cys Gln Glu Asp Ser Ala Cys Pro Ala Ala Glu Glu Ser Leu Pro Ile 195 200 205 Glu Val Met Val Asp Ala Val His Lys Leu Lys Tyr Glu Asn Tyr Thr 210 215 220 Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys Pro Asp Pro Pro Asn Asn 225 230 235 240 Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg Gln Val Glu Val Ser Trp 245 250 255 Glu Tyr Pro Asp Thr Trp Ser Thr Pro His Ser Tyr Phe Ser Leu Thr 260 265 270 Phe Cys Val Gln Val Gln Gly Lys Ser Lys Arg Glu Lys Lys Asp Arg 275 280 285 Val Phe Thr Asp Lys Thr Ser Ala Thr Val Ile Cys Arg Lys Asn Ala 290 295 300 Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr Tyr Ser Ser Ser Trp Ser 305 310 315 320 Glu Trp Ala Ser Val Pro Cys Ser Gly Gly Gly Gly Ser Gly Gly Gly 325 330 335 Gly Ser Pro Trp Arg Asn Leu Pro Val Ala Thr Pro Asp Pro Gly Met 340 345 350 Phe Pro Cys Leu His His Ser Gln Asn Leu Leu Arg Ala Val Ser Asn 355 360 365 Met Leu Gln Lys Ala Arg Gln Thr Leu Glu Phe Tyr Pro Cys Thr Ser 370 375 380 Glu Glu Ile Asp His Glu Asp Ile Thr Lys Asp Lys Thr Ser Thr Val 385 390 395 400 Glu Ala Cys Leu Pro Leu Glu Leu Thr Lys Asn Glu Ser Cys Leu Asn 405 410 415 Ser Arg Glu Thr Ser Phe Ile Thr Asn Gly Ser Cys Leu Ala Ser Arg 420 425 430 Lys Thr Ser Phe Met Met Ala Leu Cys Leu Ser Ser Ile Tyr Glu Asp 435 440 445 Leu Lys Met Tyr Gln Val Glu Phe Lys Thr Met Asn Ala Lys Leu Leu 450 455 460 Met Asp Pro Lys Arg Gln Ile Phe Leu Asp Gln Asn Met Leu Ala Val 465 470 475 480 Ile Asp Glu Leu Met Gln Ala Leu Asn Phe Asn Ser Glu Thr Val Pro 485 490 495 Gln Lys Ser Ser Leu Glu Glu Pro Asp Phe Tyr Lys Thr Lys Ile Lys 500 505 510 Leu Cys Ile Leu Leu His Ala Phe Arg Ile Arg Ala Val Thr Ile Asp 515 520 525 Arg Val Met Ser Tyr Leu Asn Ala Ser 530 535 9 8638 DNA Artificial Sequence Description of Artificial Sequence plasmid 9 tcaatattgg ccattagcca tattattcat tggttatata gcataaatca atattggcta 60 ttggccattg catacgttgt atctatatca taatatgtac atttatattg gctcatgtcc 120 aatatgaccg ccatgttggc attgattatt gactagttat taatagtaat caattacggg 180 gtcattagtt catagcccat atatggagtt ccgcgttaca taacttacgg taaatggccc 240 gcctggctga ccgcccaacg acccccgccc attgacgtca ataatgacgt atgttcccat 300 agtaacgcca atagggactt tccattgacg tcaatgggtg gagtatttac ggtaaactgc 360 ccacttggca gtacatcaag tgtatcatat gccaagtccg ccccctattg acgtcaatga 420 cggtaaatgg cccgcctggc attatgccca gtacatgacc ttacgggact ttcctacttg 480 gcagtacatc tacgtattag tcatcgctat taccatggtg atgcggtttt ggcagtacac 540 caatgggcgt ggatagcggt ttgactcacg gggatttcca agtctccacc ccattgacgt 600 caatgggagt ttgttttggc accaaaatca acgggacttt ccaaaatgtc gtaacaactg 660 cgatcgcccg ccccgttgac gcaaatgggc ggtaggcgtg tacggtggga ggtctatata 720 agcagagctc gtttagtgaa ccgtcagatc actagaagct ttattgcggt agtttatcac 780 agttaaattg ctaacgcagt cagtgcttct gacacaacag tctcgaactt aagctgcagt 840 gactctctta aggtagcctt gcagaagttg gtcgtgaggc actgggcagg taagtatcaa 900 ggttacaaga caggtttaag gagaccaata gaaactgggc ttgtcgagac agagaagact 960 cttgcgtttc tgataggcac ctattggtct tactgacatc cactttgcct ttctctccac 1020 aggtgtccac tcccagttca attacagctc ttaaggctag agtacttaat acgactcact 1080 ataggctaga tgggccacac acggaggcag ggaacatcac catccaagtg tccatacctc 1140 aatttctttc agctcttggt gctggctggt ctttctcact tctgttcagg tgttatccac 1200 gtgaccaagg aagtgaaaga agtggcaacg ctgtcctgtg gtcacaatgt ttctgttgaa 1260 gagctggcac aaactcgcat ctactggcaa aaggagaaga aaatggtgct gactatgatg 1320 tctggggaca tgaatatatg gcccgagtac aagaaccgga ccatctttga tatcactaat 1380 aacctctcca ttgtgatcct ggctctgcgc ccatctgacg agggcacata cgagtgtgtt 1440 gttctgaagt atgaaaaaga cgctttcaag cgggaacacc tggctgaagt gacgttatca 1500 gtcaaagctg acttccctac acctagtata tctgactttg aaattccaac ttctaatatt 1560 agaaggataa tttgctcaac ctctggaggt tttccagagc ctcacctctc ctggttggaa 1620 aatggagaag aattaaatgc catcaacaca acagtttccc aagatcctga aactgagctc 1680 tatgctgtta gcagcaaact ggatttcaat atgacaacca accacagctt catgtgtctc 1740 atcaagtatg gacatttaag agtgaatcag accttcaact ggaatacaac caagcaagag 1800 cattttcctg ataacctgct cccatcctgg gccattacct taatctcagt aaatggaatt 1860 tttgtgatat gctgcctgac ctactgcttt gccccaagat gcagagagag aaggaggaat 1920 gagagattga gaagggaaag tgtacgccct gtataacagt gtccgcagaa gcaaggggct 1980 gaaaacgcgt cgagcatgca tctagggcgg ccaattccgc ccctctccct cccccccccc 2040 taacgttact ggccgaagcc gcttggaata aggccggtgt gcgtttgtct atatgtgatt 2100 ttccaccata ttgccgtctt ttggcaatgt gagggcccgg aaacctggcc ctgtcttctt 2160 gacgagcatt cctaggggtc tttcccctct cgccaaagga atgcaaggtc tgttgaatgt 2220 cgtgaaggaa gcagttcctc tggaagcttc ttgaagacaa acaacgtctg tagcgaccct 2280 ttgcaggcag cggaaccccc cacctggcga caggtgcctc tgcggccaaa agccacgtgt 2340 ataagataca cctgcaaagg cggcacaacc ccagtgccac gttgtgagtt ggatagttgt 2400 ggaaagagtc aaatggctct cctcaagcgt attcaacaag gggctgaagg atgcccagaa 2460 ggtaccccat tgtatgggat ctgatctggg gcctcggtgc acatgcttta catgtgttta 2520 gtcgaggtta aaaaaacgtc taggcccccc gaaccacggg gacgtggttt tcctttgaaa 2580 aacacgatga taagcttgcc acaacccggg atcctctaga gtcgacggcc cagagcaag 2639 atg tgt cac cag cag ttg gtc atc tct tgg ttt tcc ctg gtt ttt ctg 2687 Met Cys His Gln Gln Leu Val Ile Ser Trp Phe Ser Leu Val Phe Leu 1 5 10 15 gca tct ccc ctc gtg gcc ata tgg gaa ctg aag aaa gat gtt tat gtc 2735 Ala Ser Pro Leu Val Ala Ile Trp Glu Leu Lys Lys Asp Val Tyr Val 20 25 30 gta gaa ttg gat tgg tat ccg gat gcc cct gga gaa atg gtg gtc ctc 2783 Val Glu Leu Asp Trp Tyr Pro Asp Ala Pro Gly Glu Met Val Val Leu 35 40 45 acc tgt gac acc cct gaa gaa gat ggt atc acc tgg acc ttg gac cag 2831 Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile Thr Trp Thr Leu Asp Gln 50 55 60 agc agt gag gtc tta ggc tct ggc aaa acc ctg acc atc caa gtc aaa 2879 Ser Ser Glu Val Leu Gly Ser Gly Lys Thr Leu Thr Ile Gln Val Lys 65 70 75 80 gag ttt gga gat gct ggc cag tac acc tgt cac aaa gga ggc gag gtt 2927 Glu Phe Gly Asp Ala Gly Gln Tyr Thr Cys His Lys Gly Gly Glu Val 85 90 95 cta agc cat tcg ctc ctg ctg ctt cac aaa aag gaa gat gga att tgg 2975 Leu Ser His Ser Leu Leu Leu Leu His Lys Lys Glu Asp Gly Ile Trp 100 105 110 tcc act gat att tta aag gac cag aaa gaa ccc aaa aat aag acc ttt 3023 Ser Thr Asp Ile Leu Lys Asp Gln Lys Glu Pro Lys Asn Lys Thr Phe 115 120 125 cta aga tgc gag gcc aag aat tat tct gga cgt ttc acc tgc tgg tgg 3071 Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly Arg Phe Thr Cys Trp Trp 130 135 140 ctg acg aca atc agt act gat ttg aca ttc agt gtc aaa agc agc aga 3119 Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe Ser Val Lys Ser Ser Arg 145 150 155 160 ggc tct tct gac ccc caa ggg gtg acg tgc gga gct gct aca ctc tct 3167 Gly Ser Ser Asp Pro Gln Gly Val Thr Cys Gly Ala Ala Thr Leu Ser 165 170 175 gca gag aga gtc aga ggg gac aac aag gag tat gag tac tca gtg gag 3215 Ala Glu Arg Val Arg Gly Asp Asn Lys Glu Tyr Glu Tyr Ser Val Glu 180 185 190 tgc cag gag gac agt gcc tgc cca gct gct gag gag agt ctg ccc att 3263 Cys Gln Glu Asp Ser Ala Cys Pro Ala Ala Glu Glu Ser Leu Pro Ile 195 200 205 gag gtc atg gtg gat gcc gtt cac aag ctc aag tat gaa aac tac acc 3311 Glu Val Met Val Asp Ala Val His Lys Leu Lys Tyr Glu Asn Tyr Thr 210 215 220 agc agc ttc ttc atc agg gac atc atc aaa cct gac cca ccc aac aac 3359 Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys Pro Asp Pro Pro Asn Asn 225 230 235 240 ttg cag ctg aag cca tta aag aat tct cgg cag gtg gag gtc agc tgg 3407 Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg Gln Val Glu Val Ser Trp 245 250 255 gag tac cct gac acc tgg agt act cca cat tcc tac ttc tcc ctg aca 3455 Glu Tyr Pro Asp Thr Trp Ser Thr Pro His Ser Tyr Phe Ser Leu Thr 260 265 270 ttc tgc gtt cag gtc cag ggc aag agc aag aga gaa aag aaa gat aga 3503 Phe Cys Val Gln Val Gln Gly Lys Ser Lys Arg Glu Lys Lys Asp Arg 275 280 285 gtc ttc acc gac aag acc tca gcc acg gtc atc tgc cgc aaa aat gcc 3551 Val Phe Thr Asp Lys Thr Ser Ala Thr Val Ile Cys Arg Lys Asn Ala 290 295 300 agc att agc gtg cgg gcc cag gac cgc tac tat agc tca tct tgg agc 3599 Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr Tyr Ser Ser Ser Trp Ser 305 310 315 320 gaa tgg gca tct gtg ccc tgc agt ggt ggc ggt gga agc ggt ggc ggt 3647 Glu Trp Ala Ser Val Pro Cys Ser Gly Gly Gly Gly Ser Gly Gly Gly 325 330 335 gga agc ggt ggc ggt gga agc ggt ggc ggt gga agc cca tgg aga aac 3695 Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Pro Trp Arg Asn 340 345 350 ctc ccc gtg gcc act cca gac cca gga atg ttc cca tgc ctt cac cac 3743 Leu Pro Val Ala Thr Pro Asp Pro Gly Met Phe Pro Cys Leu His His 355 360 365 tcc caa aac ctg ctg agg gcc gtc agc aac atg ctc cag aag gcc aga 3791 Ser Gln Asn Leu Leu Arg Ala Val Ser Asn Met Leu Gln Lys Ala Arg 370 375 380 caa act cta gaa ttt tac cct tgc act tct gaa gag att gat cat gaa 3839 Gln Thr Leu Glu Phe Tyr Pro Cys Thr Ser Glu Glu Ile Asp His Glu 385 390 395 400 gat atc aca aaa gat aaa acc agc aca gtg gag gcc tgt tta cca ttg 3887 Asp Ile Thr Lys Asp Lys Thr Ser Thr Val Glu Ala Cys Leu Pro Leu 405 410 415 gaa tta acc aag aat gag agt tgc cta aat tcc aga gag acc tct ttc 3935 Glu Leu Thr Lys Asn Glu Ser Cys Leu Asn Ser Arg Glu Thr Ser Phe 420 425 430 ata act aat ggg agt tgc ctg gcc tcc aga aag acc tct ttt atg atg 3983 Ile Thr Asn Gly Ser Cys Leu Ala Ser Arg Lys Thr Ser Phe Met Met 435 440 445 gcc ctg tgc ctt agt agt att tat gaa gac ttg aag atg tac cag gtg 4031 Ala Leu Cys Leu Ser Ser Ile Tyr Glu Asp Leu Lys Met Tyr Gln Val 450 455 460 gag ttc aag acc atg aat gca aag ctt ctg atg gat cct aag agg cag 4079 Glu Phe Lys Thr Met Asn Ala Lys Leu Leu Met Asp Pro Lys Arg Gln 465 470 475 480 atc ttt cta gat caa aac atg ctg gca gtt att gat gag ctg atg cag 4127 Ile Phe Leu Asp Gln Asn Met Leu Ala Val Ile Asp Glu Leu Met Gln 485 490 495 gcc ctg aat ttc aac agt gag act gtg cca caa aaa tcc tcc ctt gaa 4175 Ala Leu Asn Phe Asn Ser Glu Thr Val Pro Gln Lys Ser Ser Leu Glu 500 505 510 gaa ccg gat ttt tat aaa act aaa atc aag ctc tgc ata ctt ctt cat 4223 Glu Pro Asp Phe Tyr Lys Thr Lys Ile Lys Leu Cys Ile Leu Leu His 515 520 525 gct ttc aga att cgg gca gtg act att gat aga gtg atg agc tat ctg 4271 Ala Phe Arg Ile Arg Ala Val Thr Ile Asp Arg Val Met Ser Tyr Leu 530 535 540 aat gct tcc taa aaagcgaggt gcggccgctt ccctttagtg agggttaatg 4323 Asn Ala Ser 545 cttcgagcag acatgataag atacattgat gagtttggac aaaccacaac tagaatgcag 4383 tgaaaaaaat gctttatttg tgaaatttgt gatgctattg ctttatttgt aaccattata 4443 agctgcaata aacaagttaa caacaacaat tgcattcatt ttatgtttca ggttcagggg 4503 gagatgtggg aggtttttta aagcaagtaa aacctctaca aatgtggtaa aatccgataa 4563 ggatcgatcc gggctggcgt aatagcgaag aggcccgcac cgatcgccct tcccaacagt 4623 tgcgcagcct gaatggcgaa tggacgcgcc ctgtagcggc gcattaagcg cggcgggtgt 4683 ggtggttacg cgcagcgtga ccgctacact tgccagcgcc ctagcgcccg ctcctttcgc 4743 tttcttccct tcctttctcg ccacgttcgc cggctttccc cgtcaagctc taaatcgggg 4803 gctcccttta gggttccgat ttagagcttt acggcacctc gaccgcaaaa aacttgattt 4863 gggtgatggt tcacgtagtg ggccatcgcc ctgatagacg gtttttcgcc ctttgacgtt 4923 ggagtccacg ttctttaata gtggactctt gttccaaact ggaacaacac tcaaccctat 4983 ctcggtctat tcttttgatt tataagggat tttgccgatt tcggcctatt ggttaaaaaa 5043 tgagctgatt taacaaatat ttaacgcgaa ttttaacaaa atattaacgt ttacaatttc 5103 gcctgatgcg gtattttctc cttacgcatc tgtgcggtat ttcacaccgc atacgcggat 5163 ctgcgcagca ccatggcctg aaataacctc tgaaagagga acttggttag gtaccttctg 5223 aggcggaaag aaccagctgt ggaatgtgtg tcagttaggg tgtggaaagt ccccaggctc 5283 cccagcaggc agaagtatgc aaagcatgca tctcaattag tcagcaacca ggtgtggaaa 5343 gtccccaggc tccccagcag gcagaagtat gcaaagcatg catctcaatt agtcagcaac 5403 catagtcccg cccctaactc cgcccatccc gcccctaact ccgcccagtt ccgcccattc 5463 tccgccccat ggctgactaa ttttttttat ttatgcagag gccgaggccg cctcggcctc 5523 tgagctattc cagaagtagt gaggaggctt ttttggaggc ctaggctttt gcaaaaagct 5583 tgattcttct gacacaacag tctcgaactt aaggctagag ccaccatgat tgaacaagat 5643 ggattgcacg caggttctcc ggccgcttgg gtggagaggc tattcggcta tgactgggca 5703 caacagacaa tcggctgctc tgatgccgcc gtgttccggc tgtcagcgca ggggcgcccg 5763 gttctttttg tcaagaccga cctgtccggt gccctgaatg aactgcagga cgaggcagcg 5823 cggctatcgt ggctggccac gacgggcgtt ccttgcgcag ctgtgctcga cgttgtcact 5883 gaagcgggaa gggactggct gctattgggc gaagtgccgg ggcaggatct cctgtcatct 5943 caccttgctc ctgccgagaa agtatccatc atggctgatg caatgcggcg gctgcatacg 6003 cttgatccgg ctacctgccc attcgaccac caagcgaaac atcgcatcga gcgagcacgt 6063 actcggatgg aagccggtct tgtcgatcag gatgatctgg acgaagagca tcaggggctc 6123 gcgccagccg aactgttcgc caggctcaag gcgcgcatgc ccgacggcga ggatctcgtc 6183 gtgacccatg gcgatgcctg cttgccgaat atcatggtgg aaaatggccg cttttctgga 6243 ttcatcgact gtggccggct gggtgtggcg gaccgctatc aggacatagc gttggctacc 6303 cgtgatattg ctgaagagct tggcggcgaa tgggctgacc gcttcctcgt gctttacggt 6363 atcgccgctc ccgattcgca gcgcatcgcc ttctatcgcc ttcttgacga gttcttctga 6423 gcgggactct ggggttcgaa atgaccgacc aagcgacgcc caacctgcca tcacgatggc 6483 cgcaataaaa tatctttatt ttcattacat ctgtgtgttg gttttttgtg tgaatcgata 6543 gcgataagga tccgcgtatg gtgcactctc agtacaatct gctctgatgc cgcatagtta 6603 agccagcccc gacacccgcc aacacccgct gacgcgccct gacgggcttg tctgctcccg 6663 gcatccgctt acagacaagc tgtgaccgtc tccgggagct gcatgtgtca gaggttttca 6723 ccgtcatcac cgaaacgcgc gagacgaaag ggcctcgtga tacgcctatt tttataggtt 6783 aatgtcatga taataatggt ttcttagacg tcaggtggca cttttcgggg aaatgtgcgc 6843 ggaaccccta tttgtttatt tttctaaata cattcaaata tgtatccgct catgagacaa 6903 taaccctgat aaatgcttca ataatattga aaaaggaaga gtatgagtat tcaacatttc 6963 cgtgtcgccc ttattccctt ttttgcggca ttttgccttc ctgtttttgc tcacccagaa 7023 acgctggtga aagtaaaaga tgctgaagat cagttgggtg cacgagtggg ttacatcgaa 7083 ctggatctca acagcggtaa gatccttgag agttttcgcc ccgaagaacg ttttccaatg 7143 atgagcactt ttaaagttct gctatgtggc gcggtattat cccgtattga cgccgggcaa 7203 gagcaactcg gtcgccgcat acactattct cagaatgact tggttgagta ctcaccagtc 7263 acagaaaagc atcttacgga tggcatgaca gtaagagaat tatgcagtgc tgccataacc 7323 atgagtgata acactgcggc caacttactt ctgacaacga tcggaggacc gaaggagcta 7383 accgcttttt tgcacaacat gggggatcat gtaactcgcc ttgatcgttg ggaaccggag 7443 ctgaatgaag ccataccaaa cgacgagcgt gacaccacga tgcctgtagc aatggcaaca 7503 acgttgcgca aactattaac tggcgaacta cttactctag cttcccggca acaattaata 7563 gactggatgg aggcggataa agttgcagga ccacttctgc gctcggccct tccggctggc 7623 tggtttattg ctgataaatc tggagccggt gagcgtgggt ctcgcggtat cattgcagca 7683 ctggggccag atggtaagcc ctcccgtatc gtagttatct acacgacggg gagtcaggca 7743 actatggatg aacgaaatag acagatcgct gagataggtg cctcactgat taagcattgg 7803 taactgtcag accaagttta ctcatatata ctttagattg atttaaaact tcatttttaa 7863 tttaaaagga tctaggtgaa gatccttttt gataatctca tgaccaaaat cccttaacgt 7923 gagttttcgt tccactgagc gtcagacccc gtagaaaaga tcaaaggatc ttcttgagat 7983 cctttttttc tgcgcgtaat ctgctgcttg caaacaaaaa aaccaccgct accagcggtg 8043 gtttgtttgc cggatcaaga gctaccaact ctttttccga aggtaactgg cttcagcaga 8103 gcgcagatac caaatactgt ccttctagtg tagccgtagt taggccacca cttcaagaac 8163 tctgtagcac cgcctacata cctcgctctg ctaatcctgt taccagtggc tgctgccagt 8223 ggcgataagt cgtgtcttac cgggttggac tcaagacgat agttaccgga taaggcgcag 8283 cggtcgggct gaacgggggg ttcgtgcaca cagcccagct tggagcgaac gacctacacc 8343 gaactgagat acctacagcg tgagctatga gaaagcgcca cgcttcccga agggagaaag 8403 gcggacaggt atccggtaag cggcagggtc ggaacaggag agcgcacgag ggagcttcca 8463 gggggaaacg cctggtatct ttatagtcct gtcgggtttc gccacctctg acttgagcgt 8523 cgatttttgt gatgctcgtc aggggggcgg agcctatgga aaaacgccag caacgcggcc 8583 tttttacggt tcctggcctt ttgctggcct tttgctcaca tggctcgaca gatct 8638 10 547 PRT Artificial Sequence Description of Artificial Sequence plasmid 10 Met Cys His Gln Gln Leu Val Ile Ser Trp Phe Ser Leu Val Phe Leu 1 5 10 15 Ala Ser Pro Leu Val Ala Ile Trp Glu Leu Lys Lys Asp Val Tyr Val 20 25 30 Val Glu Leu Asp Trp Tyr Pro Asp Ala Pro Gly Glu Met Val Val Leu 35 40 45 Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile Thr Trp Thr Leu Asp Gln 50 55 60 Ser Ser Glu Val Leu Gly Ser Gly Lys Thr Leu Thr Ile Gln Val Lys 65 70 75 80 Glu Phe Gly Asp Ala Gly Gln Tyr Thr Cys His Lys Gly Gly Glu Val 85 90 95 Leu Ser His Ser Leu Leu Leu Leu His Lys Lys Glu Asp Gly Ile Trp 100 105 110 Ser Thr Asp Ile Leu Lys Asp Gln Lys Glu Pro Lys Asn Lys Thr Phe 115 120 125 Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly Arg Phe Thr Cys Trp Trp 130 135 140 Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe Ser Val Lys Ser Ser Arg 145 150 155 160 Gly Ser Ser Asp Pro Gln Gly Val Thr Cys Gly Ala Ala Thr Leu Ser 165 170 175 Ala Glu Arg Val Arg Gly Asp Asn Lys Glu Tyr Glu Tyr Ser Val Glu 180 185 190 Cys Gln Glu Asp Ser Ala Cys Pro Ala Ala Glu Glu Ser Leu Pro Ile 195 200 205 Glu Val Met Val Asp Ala Val His Lys Leu Lys Tyr Glu Asn Tyr Thr 210 215 220 Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys Pro Asp Pro Pro Asn Asn 225 230 235 240 Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg Gln Val Glu Val Ser Trp 245 250 255 Glu Tyr Pro Asp Thr Trp Ser Thr Pro His Ser Tyr Phe Ser Leu Thr 260 265 270 Phe Cys Val Gln Val Gln Gly Lys Ser Lys Arg Glu Lys Lys Asp Arg 275 280 285 Val Phe Thr Asp Lys Thr Ser Ala Thr Val Ile Cys Arg Lys Asn Ala 290 295 300 Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr Tyr Ser Ser Ser Trp Ser 305 310 315 320 Glu Trp Ala Ser Val Pro Cys Ser Gly Gly Gly Gly Ser Gly Gly Gly 325 330 335 Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Pro Trp Arg Asn 340 345 350 Leu Pro Val Ala Thr Pro Asp Pro Gly Met Phe Pro Cys Leu His His 355 360 365 Ser Gln Asn Leu Leu Arg Ala Val Ser Asn Met Leu Gln Lys Ala Arg 370 375 380 Gln Thr Leu Glu Phe Tyr Pro Cys Thr Ser Glu Glu Ile Asp His Glu 385 390 395 400 Asp Ile Thr Lys Asp Lys Thr Ser Thr Val Glu Ala Cys Leu Pro Leu 405 410 415 Glu Leu Thr Lys Asn Glu Ser Cys Leu Asn Ser Arg Glu Thr Ser Phe 420 425 430 Ile Thr Asn Gly Ser Cys Leu Ala Ser Arg Lys Thr Ser Phe Met Met 435 440 445 Ala Leu Cys Leu Ser Ser Ile Tyr Glu Asp Leu Lys Met Tyr Gln Val 450 455 460 Glu Phe Lys Thr Met Asn Ala Lys Leu Leu Met Asp Pro Lys Arg Gln 465 470 475 480 Ile Phe Leu Asp Gln Asn Met Leu Ala Val Ile Asp Glu Leu Met Gln 485 490 495 Ala Leu Asn Phe Asn Ser Glu Thr Val Pro Gln Lys Ser Ser Leu Glu 500 505 510 Glu Pro Asp Phe Tyr Lys Thr Lys Ile Lys Leu Cys Ile Leu Leu His 515 520 525 Ala Phe Arg Ile Arg Ala Val Thr Ile Asp Arg Val Met Ser Tyr Leu 530 535 540 Asn Ala Ser 545 11 8659 DNA Artificial Sequence misc_feature (1)..(750) CMV enhancer and promoter 11 tcaatattgg ccattagcca tattattcat tggttatata gcataaatca atattggcta 60 ttggccattg catacgttgt atctatatca taatatgtac atttatattg gctcatgtcc 120 aatatgaccg ccatgttggc attgattatt gactagttat taatagtaat caattacggg 180 gtcattagtt catagcccat atatggagtt ccgcgttaca taacttacgg taaatggccc 240 gcctggctga ccgcccaacg acccccgccc attgacgtca ataatgacgt atgttcccat 300 agtaacgcca atagggactt tccattgacg tcaatgggtg gagtatttac ggtaaactgc 360 ccacttggca gtacatcaag tgtatcatat gccaagtccg ccccctattg acgtcaatga 420 cggtaaatgg cccgcctggc attatgccca gtacatgacc ttacgggact ttcctacttg 480 gcagtacatc tacgtattag tcatcgctat taccatggtg atgcggtttt ggcagtacac 540 caatgggcgt ggatagcggt ttgactcacg gggatttcca agtctccacc ccattgacgt 600 caatgggagt ttgttttggc accaaaatca acgggacttt ccaaaatgtc gtaacaactg 660 cgatcgcccg ccccgttgac gcaaatgggc ggtaggcgtg tacggtggga ggtctatata 720 agcagagctc gtttagtgaa ccgtcagatc actagaagct ttattgcggt agtttatcac 780 agttaaattg ctaacgcagt cagtgcttct gacacaacag tctcgaactt aagctgcagt 840 gactctctta aggtagcctt gcagaagttg gtcgtgaggc actgggcagg taagtatcaa 900 ggttacaaga caggtttaag gagaccaata gaaactgggc ttgtcgagac agagaagact 960 cttgcgtttc tgataggcac ctattggtct tactgacatc cactttgcct ttctctccac 1020 aggtgtccac tcccagttca attacagctc ttaaggctag agtacttaat acgactcact 1080 ataggctagg gcccagagca ag atg tgt cac cag cag ttg gtc atc tct tgg 1132 Met Cys His Gln Gln Leu Val Ile Ser Trp 1 5 10 ttt tcc ctg gtt ttt ctg gca tct ccc ctc gtg gcc ata tgg gaa ctg 1180 Phe Ser Leu Val Phe Leu Ala Ser Pro Leu Val Ala Ile Trp Glu Leu 15 20 25 aag aaa gat gtt tat gtc gta gaa ttg gat tgg tat ccg gat gcc cct 1228 Lys Lys Asp Val Tyr Val Val Glu Leu Asp Trp Tyr Pro Asp Ala Pro 30 35 40 gga gaa atg gtg gtc ctc acc tgt gac acc cct gaa gaa gat ggt atc 1276 Gly Glu Met Val Val Leu Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile 45 50 55 acc tgg acc ttg gac cag agc agt gag gtc tta ggc tct ggc aaa acc 1324 Thr Trp Thr Leu Asp Gln Ser Ser Glu Val Leu Gly Ser Gly Lys Thr 60 65 70 ctg acc atc caa gtc aaa gag ttt gga gat gct ggc cag tac acc tgt 1372 Leu Thr Ile Gln Val Lys Glu Phe Gly Asp Ala Gly Gln Tyr Thr Cys 75 80 85 90 cac aaa gga ggc gag gtt cta agc cat tcg ctc ctg ctg ctt cac aaa 1420 His Lys Gly Gly Glu Val Leu Ser His Ser Leu Leu Leu Leu His Lys 95 100 105 aag gaa gat gga att tgg tcc act gat att tta aag gac cag aaa gaa 1468 Lys Glu Asp Gly Ile Trp Ser Thr Asp Ile Leu Lys Asp Gln Lys Glu 110 115 120 ccc aaa aat aag acc ttt cta aga tgc gag gcc aag aat tat tct gga 1516 Pro Lys Asn Lys Thr Phe Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly 125 130 135 cgt ttc acc tgc tgg tgg ctg acg aca atc agt act gat ttg aca ttc 1564 Arg Phe Thr Cys Trp Trp Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe 140 145 150 agt gtc aaa agc agc aga ggc tct tct gac ccc caa ggg gtg acg tgc 1612 Ser Val Lys Ser Ser Arg Gly Ser Ser Asp Pro Gln Gly Val Thr Cys 155 160 165 170 gga gct gct aca ctc tct gca gag aga gtc aga ggg gac aac aag gag 1660 Gly Ala Ala Thr Leu Ser Ala Glu Arg Val Arg Gly Asp Asn Lys Glu 175 180 185 tat gag tac tca gtg gag tgc cag gag gac agt gcc tgc cca gct gct 1708 Tyr Glu Tyr Ser Val Glu Cys Gln Glu Asp Ser Ala Cys Pro Ala Ala 190 195 200 gag gag agt ctg ccc att gag gtc atg gtg gat gcc gtt cac aag ctc 1756 Glu Glu Ser Leu Pro Ile Glu Val Met Val Asp Ala Val His Lys Leu 205 210 215 aag tat gaa aac tac acc agc agc ttc ttc atc agg gac atc atc aaa 1804 Lys Tyr Glu Asn Tyr Thr Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys 220 225 230 cct gac cca ccc aac aac ttg cag ctg aag cca tta aag aat tct cgg 1852 Pro Asp Pro Pro Asn Asn Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg 235 240 245 250 cag gtg gag gtc agc tgg gag tac cct gac acc tgg agt act cca cat 1900 Gln Val Glu Val Ser Trp Glu Tyr Pro Asp Thr Trp Ser Thr Pro His 255 260 265 tcc tac ttc tcc ctg aca ttc tgc gtt cag gtc cag ggc aag agc aag 1948 Ser Tyr Phe Ser Leu Thr Phe Cys Val Gln Val Gln Gly Lys Ser Lys 270 275 280 aga gaa aag aaa gat aga gtc ttc acc gac aag acc tca gcc acg gtc 1996 Arg Glu Lys Lys Asp Arg Val Phe Thr Asp Lys Thr Ser Ala Thr Val 285 290 295 atc tgc cgc aaa aat gcc agc att agc gtg cgg gcc cag gac cgc tac 2044 Ile Cys Arg Lys Asn Ala Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr 300 305 310 tat agc tca tct tgg agc gaa tgg gca tct gtg ccc tgc agt ggt ggc 2092 Tyr Ser Ser Ser Trp Ser Glu Trp Ala Ser Val Pro Cys Ser Gly Gly 315 320 325 330 ggt gga agc ggt ggc ggt gga agc ggt ggc ggt gga agc ggt ggc ggt 2140 Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly 335 340 345 gga agc cca tgg aga aac ctc ccc gtg gcc act cca gac cca gga atg 2188 Gly Ser Pro Trp Arg Asn Leu Pro Val Ala Thr Pro Asp Pro Gly Met 350 355 360 ttc cca tgc ctt cac cac tcc caa aac ctg ctg agg gcc gtc agc aac 2236 Phe Pro Cys Leu His His Ser Gln Asn Leu Leu Arg Ala Val Ser Asn 365 370 375 atg ctc cag aag gcc aga caa act cta gaa ttt tac cct tgc act tct 2284 Met Leu Gln Lys Ala Arg Gln Thr Leu Glu Phe Tyr Pro Cys Thr Ser 380 385 390 gaa gag att gat cat gaa gat atc aca aaa gat aaa acc agc aca gtg 2332 Glu Glu Ile Asp His Glu Asp Ile Thr Lys Asp Lys Thr Ser Thr Val 395 400 405 410 gag gcc tgt tta cca ttg gaa tta acc aag aat gag agt tgc cta aat 2380 Glu Ala Cys Leu Pro Leu Glu Leu Thr Lys Asn Glu Ser Cys Leu Asn 415 420 425 tcc aga gag acc tct ttc ata act aat ggg agt tgc ctg gcc tcc aga 2428 Ser Arg Glu Thr Ser Phe Ile Thr Asn Gly Ser Cys Leu Ala Ser Arg 430 435 440 aag acc tct ttt atg atg gcc ctg tgc ctt agt agt att tat gaa gac 2476 Lys Thr Ser Phe Met Met Ala Leu Cys Leu Ser Ser Ile Tyr Glu Asp 445 450 455 ttg aag atg tac cag gtg gag ttc aag acc atg aat gca aag ctt ctg 2524 Leu Lys Met Tyr Gln Val Glu Phe Lys Thr Met Asn Ala Lys Leu Leu 460 465 470 atg gat cct aag agg cag atc ttt cta gat caa aac atg ctg gca gtt 2572 Met Asp Pro Lys Arg Gln Ile Phe Leu Asp Gln Asn Met Leu Ala Val 475 480 485 490 att gat gag ctg atg cag gcc ctg aat ttc aac agt gag act gtg cca 2620 Ile Asp Glu Leu Met Gln Ala Leu Asn Phe Asn Ser Glu Thr Val Pro 495 500 505 caa aaa tcc tcc ctt gaa gaa ccg gat ttt tat aaa act aaa atc aag 2668 Gln Lys Ser Ser Leu Glu Glu Pro Asp Phe Tyr Lys Thr Lys Ile Lys 510 515 520 ctc tgc ata ctt ctt cat gct ttc aga att cgg gca gtg act att gat 2716 Leu Cys Ile Leu Leu His Ala Phe Arg Ile Arg Ala Val Thr Ile Asp 525 530 535 aga gtg atg agc tat ctg aat gct tcc taa aaagcgaggt acgcgtcgag 2766 Arg Val Met Ser Tyr Leu Asn Ala Ser 540 545 catgcatcta gggcggccaa ttccgcccct ctccctcccc cccccctaac gttactggcc 2826 gaagccgctt ggaataaggc cggtgtgcgt ttgtctatat gtgattttcc accatattgc 2886 cgtcttttgg caatgtgagg gcccggaaac ctggccctgt cttcttgacg agcattccta 2946 ggggtctttc ccctctcgcc aaaggaatgc aaggtctgtt gaatgtcgtg aaggaagcag 3006 ttcctctgga agcttcttga agacaaacaa cgtctgtagc gaccctttgc aggcagcgga 3066 accccccacc tggcgacagg tgcctctgcg gccaaaagcc acgtgtataa gatacacctg 3126 caaaggcggc acaaccccag tgccacgttg tgagttggat agttgtggaa agagtcaaat 3186 ggctctcctc aagcgtattc aacaaggggc tgaaggatgc ccagaaggta ccccattgta 3246 tgggatctga tctggggcct cggtgcacat gctttacatg tgtttagtcg aggttaaaaa 3306 aacgtctagg ccccccgaac cacggggacg tggttttcct ttgaaaaaca cgatgataag 3366 cttgccacaa cccgggatcc tctagagtcg acatgggcca cacacggagg cagggaacat 3426 caccatccaa gtgtccatac ctcaatttct ttcagctctt ggtgctggct ggtctttctc 3486 acttctgttc aggtgttatc cacgtgacca aggaagtgaa agaagtggca acgctgtcct 3546 gtggtcacaa tgtttctgtt gaagagctgg cacaaactcg catctactgg caaaaggaga 3606 agaaaatggt gctgactatg atgtctgggg acatgaatat atggcccgag tacaagaacc 3666 ggaccatctt tgatatcact aataacctct ccattgtgat cctggctctg cgcccatctg 3726 acgagggcac atacgagtgt gttgttctga agtatgaaaa agacgctttc aagcgggaac 3786 acctggctga agtgacgtta tcagtcaaag ctgacttccc tacacctagt atatctgact 3846 ttgaaattcc aacttctaat attagaagga taatttgctc aacctctgga ggttttccag 3906 agcctcacct ctcctggttg gaaaatggag aagaattaaa tgccatcaac acaacagttt 3966 cccaagatcc tgaaactgag ctctatgctg ttagcagcaa actggatttc aatatgacaa 4026 ccaaccacag cttcatgtgt ctcatcaagt atggacattt aagagtgaat cagaccttca 4086 actggaatac aaccaagcaa gagcattttc ctgataacct gctcccatcc tgggccatta 4146 ccttaatctc agtaaatgga atttttgtga tatgctgcct gacctactgc tttgccccaa 4206 gatgcagaga gagaaggagg aatgagagat tgagaaggga aagtgtacgc cctgtataac 4266 agtgtccgca gaagcaaggg gctgaaacgg ccgatcacta gtgaattcgc ggccgcttcc 4326 ctttagtgag ggttaatgct tcgagcagac atgataagat acattgatga gtttggacaa 4386 accacaacta gaatgcagtg aaaaaaatgc tttatttgtg aaatttgtga tgctattgct 4446 ttatttgtaa ccattataag ctgcaataaa caagttaaca acaacaattg cattcatttt 4506 atgtttcagg ttcaggggga gatgtgggag gttttttaaa gcaagtaaaa cctctacaaa 4566 tgtggtaaaa tccgataagg atcgatccgg gctggcgtaa tagcgaagag gcccgcaccg 4626 atcgcccttc ccaacagttg cgcagcctga atggcgaatg gacgcgccct gtagcggcgc 4686 attaagcgcg gcgggtgtgg tggttacgcg cagcgtgacc gctacacttg ccagcgccct 4746 agcgcccgct cctttcgctt tcttcccttc ctttctcgcc acgttcgccg gctttccccg 4806 tcaagctcta aatcgggggc tccctttagg gttccgattt agagctttac ggcacctcga 4866 ccgcaaaaaa cttgatttgg gtgatggttc acgtagtggg ccatcgccct gatagacggt 4926 ttttcgccct ttgacgttgg agtccacgtt ctttaatagt ggactcttgt tccaaactgg 4986 aacaacactc aaccctatct cggtctattc ttttgattta taagggattt tgccgatttc 5046 ggcctattgg ttaaaaaatg agctgattta acaaatattt aacgcgaatt ttaacaaaat 5106 attaacgttt acaatttcgc ctgatgcggt attttctcct tacgcatctg tgcggtattt 5166 cacaccgcat acgcggatct gcgcagcacc atggcctgaa ataacctctg aaagaggaac 5226 ttggttaggt accttctgag gcggaaagaa ccagctgtgg aatgtgtgtc agttagggtg 5286 tggaaagtcc ccaggctccc cagcaggcag aagtatgcaa agcatgcatc tcaattagtc 5346 agcaaccagg tgtggaaagt ccccaggctc cccagcaggc agaagtatgc aaagcatgca 5406 tctcaattag tcagcaacca tagtcccgcc cctaactccg cccatcccgc ccctaactcc 5466 gcccagttcc gcccattctc cgccccatgg ctgactaatt ttttttattt atgcagaggc 5526 cgaggccgcc tcggcctctg agctattcca gaagtagtga ggaggctttt ttggaggcct 5586 aggcttttgc aaaaagcttg attcttctga cacaacagtc tcgaacttaa ggctagagcc 5646 accatgattg aacaagatgg attgcacgca ggttctccgg ccgcttgggt ggagaggcta 5706 ttcggctatg actgggcaca acagacaatc ggctgctctg atgccgccgt gttccggctg 5766 tcagcgcagg ggcgcccggt tctttttgtc aagaccgacc tgtccggtgc cctgaatgaa 5826 ctgcaggacg aggcagcgcg gctatcgtgg ctggccacga cgggcgttcc ttgcgcagct 5886 gtgctcgacg ttgtcactga agcgggaagg gactggctgc tattgggcga agtgccgggg 5946 caggatctcc tgtcatctca ccttgctcct gccgagaaag tatccatcat ggctgatgca 6006 atgcggcggc tgcatacgct tgatccggct acctgcccat tcgaccacca agcgaaacat 6066 cgcatcgagc gagcacgtac tcggatggaa gccggtcttg tcgatcagga tgatctggac 6126 gaagagcatc aggggctcgc gccagccgaa ctgttcgcca ggctcaaggc gcgcatgccc 6186 gacggcgagg atctcgtcgt gacccatggc gatgcctgct tgccgaatat catggtggaa 6246 aatggccgct tttctggatt catcgactgt ggccggctgg gtgtggcgga ccgctatcag 6306 gacatagcgt tggctacccg tgatattgct gaagagcttg gcggcgaatg ggctgaccgc 6366 ttcctcgtgc tttacggtat cgccgctccc gattcgcagc gcatcgcctt ctatcgcctt 6426 cttgacgagt tcttctgagc gggactctgg ggttcgaaat gaccgaccaa gcgacgccca 6486 acctgccatc acgatggccg caataaaata tctttatttt cattacatct gtgtgttggt 6546 tttttgtgtg aatcgatagc gataaggatc cgcgtatggt gcactctcag tacaatctgc 6606 tctgatgccg catagttaag ccagccccga cacccgccaa cacccgctga cgcgccctga 6666 cgggcttgtc tgctcccggc atccgcttac agacaagctg tgaccgtctc cgggagctgc 6726 atgtgtcaga ggttttcacc gtcatcaccg aaacgcgcga gacgaaaggg cctcgtgata 6786 cgcctatttt tataggttaa tgtcatgata ataatggttt cttagacgtc aggtggcact 6846 tttcggggaa atgtgcgcgg aacccctatt tgtttatttt tctaaataca ttcaaatatg 6906 tatccgctca tgagacaata accctgataa atgcttcaat aatattgaaa aaggaagagt 6966 atgagtattc aacatttccg tgtcgccctt attccctttt ttgcggcatt ttgccttcct 7026 gtttttgctc acccagaaac gctggtgaaa gtaaaagatg ctgaagatca gttgggtgca 7086 cgagtgggtt acatcgaact ggatctcaac agcggtaaga tccttgagag ttttcgcccc 7146 gaagaacgtt ttccaatgat gagcactttt aaagttctgc tatgtggcgc ggtattatcc 7206 cgtattgacg ccgggcaaga gcaactcggt cgccgcatac actattctca gaatgacttg 7266 gttgagtact caccagtcac agaaaagcat cttacggatg gcatgacagt aagagaatta 7326 tgcagtgctg ccataaccat gagtgataac actgcggcca acttacttct gacaacgatc 7386 ggaggaccga aggagctaac cgcttttttg cacaacatgg gggatcatgt aactcgcctt 7446 gatcgttggg aaccggagct gaatgaagcc ataccaaacg acgagcgtga caccacgatg 7506 cctgtagcaa tggcaacaac gttgcgcaaa ctattaactg gcgaactact tactttagct 7566 tcccggcaac aattaataga ctggatggag gcggataaag ttgcaggacc acttctgcgc 7626 tcggcccttc cggctggctg gtttattgct gataaatctg gagccggtga gcgtgggtct 7686 cgcggtatca ttgcagcact ggggccagat ggtaagccct cccgtatcgt agttatctac 7746 acgacgggga gtcaggcaac tatggatgaa cgaaatagac agatcgctga gataggtgcc 7806 tcactgatta agcattggta actgtcagac caagtttact catatatact ttagattgat 7866 ttaaaacttc atttttaatt taaaaggatc taggtgaaga tcctttttga taatctcatg 7926 accaaaatcc cttaacgtga gttttcgttc cactgagcgt cagaccccgt agaaaagatc 7986 aaaggatctt cttgagatcc tttttttctg cgcgtaatct gctgcttgca aacaaaaaaa 8046 ccaccgctac cagcggtggt ttgtttgccg gatcaagagc taccaactct ttttccgaag 8106 gtaactggct tcagcagagc gcagatacca aatactgtcc ttctagtgta gccgtagtta 8166 ggccaccact tcaagaactc tgtagcaccg cctacatacc tcgctctgct aatcctgtta 8226 ccagtggctg ctgccagtgg cgataagtcg tgtcttaccg ggttggactc aagacgatag 8286 ttaccggata aggcgcagcg gtcgggctga acggggggtt cgtgcacaca gcccagcttg 8346 gagcgaacga cctacaccga actgagatac ctacagcgtg agctatgaga aagcgccacg 8406 cttcccgaag ggagaaaggc ggacaggtat ccggtaagcg gcagggtcgg aacaggagag 8466 cgcacgaggg agcttccagg gggaaacgcc tggtatcttt atagtcctgt cgggtttcgc 8526 cacctctgac ttgagcgtcg atttttgtga tgctcgtcag gggggcggag cctatggaaa 8586 aacgccagca acgcggcctt tttacggttc ctggcctttt gctggccttt tgctcacatg 8646 gctcgacaga tct 8659 12 547 PRT Artificial Sequence Description of Artificial Sequence plasmid 12 Met Cys His Gln Gln Leu Val Ile Ser Trp Phe Ser Leu Val Phe Leu 1 5 10 15 Ala Ser Pro Leu Val Ala Ile Trp Glu Leu Lys Lys Asp Val Tyr Val 20 25 30 Val Glu Leu Asp Trp Tyr Pro Asp Ala Pro Gly Glu Met Val Val Leu 35 40 45 Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile Thr Trp Thr Leu Asp Gln 50 55 60 Ser Ser Glu Val Leu Gly Ser Gly Lys Thr Leu Thr Ile Gln Val Lys 65 70 75 80 Glu Phe Gly Asp Ala Gly Gln Tyr Thr Cys His Lys Gly Gly Glu Val 85 90 95 Leu Ser His Ser Leu Leu Leu Leu His Lys Lys Glu Asp Gly Ile Trp 100 105 110 Ser Thr Asp Ile Leu Lys Asp Gln Lys Glu Pro Lys Asn Lys Thr Phe 115 120 125 Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly Arg Phe Thr Cys Trp Trp 130 135 140 Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe Ser Val Lys Ser Ser Arg 145 150 155 160 Gly Ser Ser Asp Pro Gln Gly Val Thr Cys Gly Ala Ala Thr Leu Ser 165 170 175 Ala Glu Arg Val Arg Gly Asp Asn Lys Glu Tyr Glu Tyr Ser Val Glu 180 185 190 Cys Gln Glu Asp Ser Ala Cys Pro Ala Ala Glu Glu Ser Leu Pro Ile 195 200 205 Glu Val Met Val Asp Ala Val His Lys Leu Lys Tyr Glu Asn Tyr Thr 210 215 220 Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys Pro Asp Pro Pro Asn Asn 225 230 235 240 Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg Gln Val Glu Val Ser Trp 245 250 255 Glu Tyr Pro Asp Thr Trp Ser Thr Pro His Ser Tyr Phe Ser Leu Thr 260 265 270 Phe Cys Val Gln Val Gln Gly Lys Ser Lys Arg Glu Lys Lys Asp Arg 275 280 285 Val Phe Thr Asp Lys Thr Ser Ala Thr Val Ile Cys Arg Lys Asn Ala 290 295 300 Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr Tyr Ser Ser Ser Trp Ser 305 310 315 320 Glu Trp Ala Ser Val Pro Cys Ser Gly Gly Gly Gly Ser Gly Gly Gly 325 330 335 Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Pro Trp Arg Asn 340 345 350 Leu Pro Val Ala Thr Pro Asp Pro Gly Met Phe Pro Cys Leu His His 355 360 365 Ser Gln Asn Leu Leu Arg Ala Val Ser Asn Met Leu Gln Lys Ala Arg 370 375 380 Gln Thr Leu Glu Phe Tyr Pro Cys Thr Ser Glu Glu Ile Asp His Glu 385 390 395 400 Asp Ile Thr Lys Asp Lys Thr Ser Thr Val Glu Ala Cys Leu Pro Leu 405 410 415 Glu Leu Thr Lys Asn Glu Ser Cys Leu Asn Ser Arg Glu Thr Ser Phe 420 425 430 Ile Thr Asn Gly Ser Cys Leu Ala Ser Arg Lys Thr Ser Phe Met Met 435 440 445 Ala Leu Cys Leu Ser Ser Ile Tyr Glu Asp Leu Lys Met Tyr Gln Val 450 455 460 Glu Phe Lys Thr Met Asn Ala Lys Leu Leu Met Asp Pro Lys Arg Gln 465 470 475 480 Ile Phe Leu Asp Gln Asn Met Leu Ala Val Ile Asp Glu Leu Met Gln 485 490 495 Ala Leu Asn Phe Asn Ser Glu Thr Val Pro Gln Lys Ser Ser Leu Glu 500 505 510 Glu Pro Asp Phe Tyr Lys Thr Lys Ile Lys Leu Cys Ile Leu Leu His 515 520 525 Ala Phe Arg Ile Arg Ala Val Thr Ile Asp Arg Val Met Ser Tyr Leu 530 535 540 Asn Ala Ser 545 13 8644 DNA Artificial Sequence Description of Artificial Sequence plasmid 13 tcaatattgg ccattagcca tattattcat tggttatata gcataaatca atattggcta 60 ttggccattg catacgttgt atctatatca taatatgtac atttatattg gctcatgtcc 120 aatatgaccg ccatgttggc attgattatt gactagttat taatagtaat caattacggg 180 gtcattagtt catagcccat atatggagtt ccgcgttaca taacttacgg taaatggccc 240 gcctggctga ccgcccaacg acccccgccc attgacgtca ataatgacgt atgttcccat 300 agtaacgcca atagggactt tccattgacg tcaatgggtg gagtatttac ggtaaactgc 360 ccacttggca gtacatcaag tgtatcatat gccaagtccg ccccctattg acgtcaatga 420 cggtaaatgg cccgcctggc attatgccca gtacatgacc ttacgggact ttcctacttg 480 gcagtacatc tacgtattag tcatcgctat taccatggtg atgcggtttt ggcagtacac 540 caatgggcgt ggatagcggt ttgactcacg gggatttcca agtctccacc ccattgacgt 600 caatgggagt ttgttttggc accaaaatca acgggacttt ccaaaatgtc gtaacaactg 660 cgatcgcccg ccccgttgac gcaaatgggc ggtaggcgtg tacggtggga ggtctatata 720 agcagagctc gtttagtgaa ccgtcagatc actagaagct ttattgcggt agtttatcac 780 agttaaattg ctaacgcagt cagtgcttct gacacaacag tctcgaactt aagctgcagt 840 gactctctta aggtagcctt gcagaagttg gtcgtgaggc actgggcagg taagtatcaa 900 ggttacaaga caggtttaag gagaccaata gaaactgggc ttgtcgagac agagaagact 960 cttgcgtttc tgataggcac ctattggtct tactgacatc cactttgcct ttctctccac 1020 aggtgtccac tcccagttca attacagctc ttaaggctag agtacttaat acgactcact 1080 ataggctagg gcccagagca ag atg tgt cac cag cag ttg gtc atc tct tgg 1132 Met Cys His Gln Gln Leu Val Ile Ser Trp 1 5 10 ttt tcc ctg gtt ttt ctg gca tct ccc ctc gtg gcc ata tgg gaa ctg 1180 Phe Ser Leu Val Phe Leu Ala Ser Pro Leu Val Ala Ile Trp Glu Leu 15 20 25 aag aaa gat gtt tat gtc gta gaa ttg gat tgg tat ccg gat gcc cct 1228 Lys Lys Asp Val Tyr Val Val Glu Leu Asp Trp Tyr Pro Asp Ala Pro 30 35 40 gga gaa atg gtg gtc ctc acc tgt gac acc cct gaa gaa gat ggt atc 1276 Gly Glu Met Val Val Leu Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile 45 50 55 acc tgg acc ttg gac cag agc agt gag gtc tta ggc tct ggc aaa acc 1324 Thr Trp Thr Leu Asp Gln Ser Ser Glu Val Leu Gly Ser Gly Lys Thr 60 65 70 ctg acc atc caa gtc aaa gag ttt gga gat gct ggc cag tac acc tgt 1372 Leu Thr Ile Gln Val Lys Glu Phe Gly Asp Ala Gly Gln Tyr Thr Cys 75 80 85 90 cac aaa gga ggc gag gtt cta agc cat tcg ctc ctg ctg ctt cac aaa 1420 His Lys Gly Gly Glu Val Leu Ser His Ser Leu Leu Leu Leu His Lys 95 100 105 aag gaa gat gga att tgg tcc act gat att tta aag gac cag aaa gaa 1468 Lys Glu Asp Gly Ile Trp Ser Thr Asp Ile Leu Lys Asp Gln Lys Glu 110 115 120 ccc aaa aat aag acc ttt cta aga tgc gag gcc aag aat tat tct gga 1516 Pro Lys Asn Lys Thr Phe Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly 125 130 135 cgt ttc acc tgc tgg tgg ctg acg aca atc agt act gat ttg aca ttc 1564 Arg Phe Thr Cys Trp Trp Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe 140 145 150 agt gtc aaa agc agc aga ggc tct tct gac ccc caa ggg gtg acg tgc 1612 Ser Val Lys Ser Ser Arg Gly Ser Ser Asp Pro Gln Gly Val Thr Cys 155 160 165 170 gga gct gct aca ctc tct gca gag aga gtc aga ggg gac aac aag gag 1660 Gly Ala Ala Thr Leu Ser Ala Glu Arg Val Arg Gly Asp Asn Lys Glu 175 180 185 tat gag tac tca gtg gag tgc cag gag gac agt gcc tgc cca gct gct 1708 Tyr Glu Tyr Ser Val Glu Cys Gln Glu Asp Ser Ala Cys Pro Ala Ala 190 195 200 gag gag agt ctg ccc att gag gtc atg gtg gat gcc gtt cac aag ctc 1756 Glu Glu Ser Leu Pro Ile Glu Val Met Val Asp Ala Val His Lys Leu 205 210 215 aag tat gaa aac tac acc agc agc ttc ttc atc agg gac atc atc aaa 1804 Lys Tyr Glu Asn Tyr Thr Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys 220 225 230 cct gac cca ccc aac aac ttg cag ctg aag cca tta aag aat tct cgg 1852 Pro Asp Pro Pro Asn Asn Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg 235 240 245 250 cag gtg gag gtc agc tgg gag tac cct gac acc tgg agt act cca cat 1900 Gln Val Glu Val Ser Trp Glu Tyr Pro Asp Thr Trp Ser Thr Pro His 255 260 265 tcc tac ttc tcc ctg aca ttc tgc gtt cag gtc cag ggc aag agc aag 1948 Ser Tyr Phe Ser Leu Thr Phe Cys Val Gln Val Gln Gly Lys Ser Lys 270 275 280 aga gaa aag aaa gat aga gtc ttc acc gac aag acc tca gcc acg gtc 1996 Arg Glu Lys Lys Asp Arg Val Phe Thr Asp Lys Thr Ser Ala Thr Val 285 290 295 atc tgc cgc aaa aat gcc agc att agc gtg cgg gcc cag gac cgc tac 2044 Ile Cys Arg Lys Asn Ala Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr 300 305 310 tat agc tca tct tgg agc gaa tgg gca tct gtg ccc tgc agt ggt ggc 2092 Tyr Ser Ser Ser Trp Ser Glu Trp Ala Ser Val Pro Cys Ser Gly Gly 315 320 325 330 ggt gga agc ggt ggc ggt gga agc ggt ggc ggt gga agc cca tgg aga 2140 Gly Gly Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Pro Trp Arg 335 340 345 aac ctc ccc gtg gcc act cca gac cca gga atg ttc cca tgc ctt cac 2188 Asn Leu Pro Val Ala Thr Pro Asp Pro Gly Met Phe Pro Cys Leu His 350 355 360 cac tcc caa aac ctg ctg agg gcc gtc agc aac atg ctc cag aag gcc 2236 His Ser Gln Asn Leu Leu Arg Ala Val Ser Asn Met Leu Gln Lys Ala 365 370 375 aga caa act cta gaa ttt tac cct tgc act tct gaa gag att gat cat 2284 Arg Gln Thr Leu Glu Phe Tyr Pro Cys Thr Ser Glu Glu Ile Asp His 380 385 390 gaa gat atc aca aaa gat aaa acc agc aca gtg gag gcc tgt tta cca 2332 Glu Asp Ile Thr Lys Asp Lys Thr Ser Thr Val Glu Ala Cys Leu Pro 395 400 405 410 ttg gaa tta acc aag aat gag agt tgc cta aat tcc aga gag acc tct 2380 Leu Glu Leu Thr Lys Asn Glu Ser Cys Leu Asn Ser Arg Glu Thr Ser 415 420 425 ttc ata act aat ggg agt tgc ctg gcc tcc aga aag acc tct ttt atg 2428 Phe Ile Thr Asn Gly Ser Cys Leu Ala Ser Arg Lys Thr Ser Phe Met 430 435 440 atg gcc ctg tgc ctt agt agt att tat gaa gac ttg aag atg tac cag 2476 Met Ala Leu Cys Leu Ser Ser Ile Tyr Glu Asp Leu Lys Met Tyr Gln 445 450 455 gtg gag ttc aag acc atg aat gca aag ctt ctg atg gat cct aag agg 2524 Val Glu Phe Lys Thr Met Asn Ala Lys Leu Leu Met Asp Pro Lys Arg 460 465 470 cag atc ttt cta gat caa aac atg ctg gca gtt att gat gag ctg atg 2572 Gln Ile Phe Leu Asp Gln Asn Met Leu Ala Val Ile Asp Glu Leu Met 475 480 485 490 cag gcc ctg aat ttc aac agt gag act gtg cca caa aaa tcc tcc ctt 2620 Gln Ala Leu Asn Phe Asn Ser Glu Thr Val Pro Gln Lys Ser Ser Leu 495 500 505 gaa gaa ccg gat ttt tat aaa act aaa atc aag ctc tgc ata ctt ctt 2668 Glu Glu Pro Asp Phe Tyr Lys Thr Lys Ile Lys Leu Cys Ile Leu Leu 510 515 520 cat gct ttc aga att cgg gca gtg act att gat aga gtg atg agc tat 2716 His Ala Phe Arg Ile Arg Ala Val Thr Ile Asp Arg Val Met Ser Tyr 525 530 535 ctg aat gct tcc taa aaagcgaggt acgcgtcgag catgcatcta gggcggccaa 2771 Leu Asn Ala Ser 540 ttccgcccct ctccctcccc cccccctaac gttactggcc gaagccgctt ggaataaggc 2831 cggtgtgcgt ttgtctatat gtgattttcc accatattgc cgtcttttgg caatgtgagg 2891 gcccggaaac ctggccctgt cttcttgacg agcattccta ggggtctttc ccctctcgcc 2951 aaaggaatgc aaggtctgtt gaatgtcgtg aaggaagcag ttcctctgga agcttcttga 3011 agacaaacaa cgtctgtagc gaccctttgc aggcagcgga accccccacc tggcgacagg 3071 tgcctctgcg gccaaaagcc acgtgtataa gatacacctg caaaggcggc acaaccccag 3131 tgccacgttg tgagttggat agttgtggaa agagtcaaat ggctctcctc aagcgtattc 3191 aacaaggggc tgaaggatgc ccagaaggta ccccattgta tgggatctga tctggggcct 3251 cggtgcacat gctttacatg tgtttagtcg aggttaaaaa aacgtctagg ccccccgaac 3311 cacggggacg tggttttcct ttgaaaaaca cgatgataag cttgccacaa cccgggatcc 3371 tctagagtcg acatgggcca cacacggagg cagggaacat caccatccaa gtgtccatac 3431 ctcaatttct ttcagctctt ggtgctggct ggtctttctc acttctgttc aggtgttatc 3491 cacgtgacca aggaagtgaa agaagtggca acgctgtcct gtggtcacaa tgtttctgtt 3551 gaagagctgg cacaaactcg catctactgg caaaaggaga agaaaatggt gctgactatg 3611 atgtctgggg acatgaatat atggcccgag tacaagaacc ggaccatctt tgatatcact 3671 aataacctct ccattgtgat cctggctctg cgcccatctg acgagggcac atacgagtgt 3731 gttgttctga agtatgaaaa agacgctttc aagcgggaac acctggctga agtgacgtta 3791 tcagtcaaag ctgacttccc tacacctagt atatctgact ttgaaattcc aacttctaat 3851 attagaagga taatttgctc aacctctgga ggttttccag agcctcacct ctcctggttg 3911 gaaaatggag aagaattaaa tgccatcaac acaacagttt cccaagatcc tgaaactgag 3971 ctctatgctg ttagcagcaa actggatttc aatatgacaa ccaaccacag cttcatgtgt 4031 ctcatcaagt atggacattt aagagtgaat cagaccttca actggaatac aaccaagcaa 4091 gagcattttc ctgataacct gctcccatcc tgggccatta ccttaatctc agtaaatgga 4151 atttttgtga tatgctgcct gacctactgc tttgccccaa gatgcagaga gagaaggagg 4211 aatgagagat tgagaaggga aagtgtacgc cctgtataac agtgtccgca gaagcaaggg 4271 gctgaaacgg ccgatcacta gtgaattcgc ggccgcttcc ctttagtgag ggttaatgct 4331 tcgagcagac atgataagat acattgatga gtttggacaa accacaacta gaatgcagtg 4391 aaaaaaatgc tttatttgtg aaatttgtga tgctattgct ttatttgtaa ccattataag 4451 ctgcaataaa caagttaaca acaacaattg cattcatttt atgtttcagg ttcaggggga 4511 gatgtgggag gttttttaaa gcaagtaaaa cctctacaaa tgtggtaaaa tccgataagg 4571 atcgatccgg gctggcgtaa tagcgaagag gcccgcaccg atcgcccttc ccaacagttg 4631 cgcagcctga atggcgaatg gacgcgccct gtagcggcgc attaagcgcg gcgggtgtgg 4691 tggttacgcg cagcgtgacc gctacacttg ccagcgccct agcgcccgct cctttcgctt 4751 tcttcccttc ctttctcgcc acgttcgccg gctttccccg tcaagctcta aatcgggggc 4811 tccctttagg gttccgattt agagctttac ggcacctcga ccgcaaaaaa cttgatttgg 4871 gtgatggttc acgtagtggg ccatcgccct gatagacggt ttttcgccct ttgacgttgg 4931 agtccacgtt ctttaatagt ggactcttgt tccaaactgg aacaacactc aaccctatct 4991 cggtctattc ttttgattta taagggattt tgccgatttc ggcctattgg ttaaaaaatg 5051 agctgattta acaaatattt aacgcgaatt ttaacaaaat attaacgttt acaatttcgc 5111 ctgatgcggt attttctcct tacgcatctg tgcggtattt cacaccgcat acgcggatct 5171 gcgcagcacc atggcctgaa ataacctctg aaagaggaac ttggttaggt accttctgag 5231 gcggaaagaa ccagctgtgg aatgtgtgtc agttagggtg tggaaagtcc ccaggctccc 5291 cagcaggcag aagtatgcaa agcatgcatc tcaattagtc agcaaccagg tgtggaaagt 5351 ccccaggctc cccagcaggc agaagtatgc aaagcatgca tctcaattag tcagcaacca 5411 tagtcccgcc cctaactccg cccatcccgc ccctaactcc gcccagttcc gcccattctc 5471 cgccccatgg ctgactaatt ttttttattt atgcagaggc cgaggccgcc tcggcctctg 5531 agctattcca gaagtagtga ggaggctttt ttggaggcct aggcttttgc aaaaagcttg 5591 attcttctga cacaacagtc tcgaacttaa ggctagagcc accatgattg aacaagatgg 5651 attgcacgca ggttctccgg ccgcttgggt ggagaggcta ttcggctatg actgggcaca 5711 acagacaatc ggctgctctg atgccgccgt gttccggctg tcagcgcagg ggcgcccggt 5771 tctttttgtc aagaccgacc tgtccggtgc cctgaatgaa ctgcaggacg aggcagcgcg 5831 gctatcgtgg ctggccacga cgggcgttcc ttgcgcagct gtgctcgacg ttgtcactga 5891 agcgggaagg gactggctgc tattgggcga agtgccgggg caggatctcc tgtcatctca 5951 ccttgctcct gccgagaaag tatccatcat ggctgatgca atgcggcggc tgcatacgct 6011 tgatccggct acctgcccat tcgaccacca agcgaaacat cgcatcgagc gagcacgtac 6071 tcggatggaa gccggtcttg tcgatcagga tgatctggac gaagagcatc aggggctcgc 6131 gccagccgaa ctgttcgcca ggctcaaggc gcgcatgccc gacggcgagg atctcgtcgt 6191 gacccatggc gatgcctgct tgccgaatat catggtggaa aatggccgct tttctggatt 6251 catcgactgt ggccggctgg gtgtggcgga ccgctatcag gacatagcgt tggctacccg 6311 tgatattgct gaagagcttg gcggcgaatg ggctgaccgc ttcctcgtgc tttacggtat 6371 cgccgctccc gattcgcagc gcatcgcctt ctatcgcctt cttgacgagt tcttctgagc 6431 gggactctgg ggttcgaaat gaccgaccaa gcgacgccca acctgccatc acgatggccg 6491 caataaaata tctttatttt cattacatct gtgtgttggt tttttgtgtg aatcgatagc 6551 gataaggatc cgcgtatggt gcactctcag tacaatctgc tctgatgccg catagttaag 6611 ccagccccga cacccgccaa cacccgctga cgcgccctga cgggcttgtc tgctcccggc 6671 atccgcttac agacaagctg tgaccgtctc cgggagctgc atgtgtcaga ggttttcacc 6731 gtcatcaccg aaacgcgcga gacgaaaggg cctcgtgata cgcctatttt tataggttaa 6791 tgtcatgata ataatggttt cttagacgtc aggtggcact tttcggggaa atgtgcgcgg 6851 aacccctatt tgtttatttt tctaaataca ttcaaatatg tatccgctca tgagacaata 6911 accctgataa atgcttcaat aatattgaaa aaggaagagt atgagtattc aacatttccg 6971 tgtcgccctt attccctttt ttgcggcatt ttgccttcct gtttttgctc acccagaaac 7031 gctggtgaaa gtaaaagatg ctgaagatca gttgggtgca cgagtgggtt acatcgaact 7091 ggatctcaac agcggtaaga tccttgagag ttttcgcccc gaagaacgtt ttccaatgat 7151 gagcactttt aaagttctgc tatgtggcgc ggtattatcc cgtattgacg ccgggcaaga 7211 gcaactcggt cgccgcatac actattctca gaatgacttg gttgagtact caccagtcac 7271 agaaaagcat cttacggatg gcatgacagt aagagaatta tgcagtgctg ccataaccat 7331 gagtgataac actgcggcca acttacttct gacaacgatc ggaggaccga aggagctaac 7391 cgcttttttg cacaacatgg gggatcatgt aactcgcctt gatcgttggg aaccggagct 7451 gaatgaagcc ataccaaacg acgagcgtga caccacgatg cctgtagcaa tggcaacaac 7511 gttgcgcaaa ctattaactg gcgaactact tactctagct tcccggcaac aattaataga 7571 ctggatggag gcggataaag ttgcaggacc acttctgcgc tcggcccttc cggctggctg 7631 gtttattgct gataaatctg gagccggtga gcgtgggtct cgcggtatca ttgcagcact 7691 ggggccagat ggtaagccct cccgtatcgt agttatctac acgacgggga gtcaggcaac 7751 tatggatgaa cgaaatagac agatcgctga gataggtgcc tcactgatta agcattggta 7811 actgtcagac caagtttact catatatact ttagattgat ttaaaacttc atttttaatt 7871 taaaaggatc taggtgaaga tcctttttga taatctcatg accaaaatcc cttaacgtga 7931 gttttcgttc cactgagcgt cagaccccgt agaaaagatc aaaggatctt cttgagatcc 7991 tttttttctg cgcgtaatct gctgcttgca aacaaaaaaa ccaccgctac cagcggtggt 8051 ttgtttgccg gatcaagagc taccaactct ttttccgaag gtaactggct tcagcagagc 8111 gcagatacca aatactgtcc ttctagtgta gccgtagtta ggccaccact tcaagaactc 8171 tgtagcaccg cctacatacc tcgctctgct aatcctgtta ccagtggctg ctgccagtgg 8231 cgataagtcg tgtcttaccg ggttggactc aagacgatag ttaccggata aggcgcagcg 8291 gtcgggctga acggggggtt cgtgcacaca gcccagcttg gagcgaacga cctacaccga 8351 actgagatac ctacagcgtg agctatgaga aagcgccacg cttcccgaag ggagaaaggc 8411 ggacaggtat ccggtaagcg gcagggtcgg aacaggagag cgcacgaggg agcttccagg 8471 gggaaacgcc tggtatcttt atagtcctgt cgggtttcgc cacctctgac ttgagcgtcg 8531 atttttgtga tgctcgtcag gggggcggag cctatggaaa aacgccagca acgcggcctt 8591 tttacggttc ctggcctttt gctggccttt tgctcacatg gctcgacaga tct 8644 14 542 PRT Artificial Sequence Description of Artificial Sequence plasmid 14 Met Cys His Gln Gln Leu Val Ile Ser Trp Phe Ser Leu Val Phe Leu 1 5 10 15 Ala Ser Pro Leu Val Ala Ile Trp Glu Leu Lys Lys Asp Val Tyr Val 20 25 30 Val Glu Leu Asp Trp Tyr Pro Asp Ala Pro Gly Glu Met Val Val Leu 35 40 45 Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile Thr Trp Thr Leu Asp Gln 50 55 60 Ser Ser Glu Val Leu Gly Ser Gly Lys Thr Leu Thr Ile Gln Val Lys 65 70 75 80 Glu Phe Gly Asp Ala Gly Gln Tyr Thr Cys His Lys Gly Gly Glu Val 85 90 95 Leu Ser His Ser Leu Leu Leu Leu His Lys Lys Glu Asp Gly Ile Trp 100 105 110 Ser Thr Asp Ile Leu Lys Asp Gln Lys Glu Pro Lys Asn Lys Thr Phe 115 120 125 Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly Arg Phe Thr Cys Trp Trp 130 135 140 Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe Ser Val Lys Ser Ser Arg 145 150 155 160 Gly Ser Ser Asp Pro Gln Gly Val Thr Cys Gly Ala Ala Thr Leu Ser 165 170 175 Ala Glu Arg Val Arg Gly Asp Asn Lys Glu Tyr Glu Tyr Ser Val Glu 180 185 190 Cys Gln Glu Asp Ser Ala Cys Pro Ala Ala Glu Glu Ser Leu Pro Ile 195 200 205 Glu Val Met Val Asp Ala Val His Lys Leu Lys Tyr Glu Asn Tyr Thr 210 215 220 Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys Pro Asp Pro Pro Asn Asn 225 230 235 240 Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg Gln Val Glu Val Ser Trp 245 250 255 Glu Tyr Pro Asp Thr Trp Ser Thr Pro His Ser Tyr Phe Ser Leu Thr 260 265 270 Phe Cys Val Gln Val Gln Gly Lys Ser Lys Arg Glu Lys Lys Asp Arg 275 280 285 Val Phe Thr Asp Lys Thr Ser Ala Thr Val Ile Cys Arg Lys Asn Ala 290 295 300 Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr Tyr Ser Ser Ser Trp Ser 305 310 315 320 Glu Trp Ala Ser Val Pro Cys Ser Gly Gly Gly Gly Ser Gly Gly Gly 325 330 335 Gly Ser Gly Gly Gly Gly Ser Pro Trp Arg Asn Leu Pro Val Ala Thr 340 345 350 Pro Asp Pro Gly Met Phe Pro Cys Leu His His Ser Gln Asn Leu Leu 355 360 365 Arg Ala Val Ser Asn Met Leu Gln Lys Ala Arg Gln Thr Leu Glu Phe 370 375 380 Tyr Pro Cys Thr Ser Glu Glu Ile Asp His Glu Asp Ile Thr Lys Asp 385 390 395 400 Lys Thr Ser Thr Val Glu Ala Cys Leu Pro Leu Glu Leu Thr Lys Asn 405 410 415 Glu Ser Cys Leu Asn Ser Arg Glu Thr Ser Phe Ile Thr Asn Gly Ser 420 425 430 Cys Leu Ala Ser Arg Lys Thr Ser Phe Met Met Ala Leu Cys Leu Ser 435 440 445 Ser Ile Tyr Glu Asp Leu Lys Met Tyr Gln Val Glu Phe Lys Thr Met 450 455 460 Asn Ala Lys Leu Leu Met Asp Pro Lys Arg Gln Ile Phe Leu Asp Gln 465 470 475 480 Asn Met Leu Ala Val Ile Asp Glu Leu Met Gln Ala Leu Asn Phe Asn 485 490 495 Ser Glu Thr Val Pro Gln Lys Ser Ser Leu Glu Glu Pro Asp Phe Tyr 500 505 510 Lys Thr Lys Ile Lys Leu Cys Ile Leu Leu His Ala Phe Arg Ile Arg 515 520 525 Ala Val Thr Ile Asp Arg Val Met Ser Tyr Leu Asn Ala Ser 530 535 540 15 8629 DNA Artificial Sequence Description of Artificial Sequence plasmid 15 tcaatattgg ccattagcca tattattcat tggttatata gcataaatca atattggcta 60 ttggccattg catacgttgt atctatatca taatatgtac atttatattg gctcatgtcc 120 aatatgaccg ccatgttggc attgattatt gactagttat taatagtaat caattacggg 180 gtcattagtt catagcccat atatggagtt ccgcgttaca taacttacgg taaatggccc 240 gcctggctga ccgcccaacg acccccgccc attgacgtca ataatgacgt atgttcccat 300 agtaacgcca atagggactt tccattgacg tcaatgggtg gagtatttac ggtaaactgc 360 ccacttggca gtacatcaag tgtatcatat gccaagtccg ccccctattg acgtcaatga 420 cggtaaatgg cccgcctggc attatgccca gtacatgacc ttacgggact ttcctacttg 480 gcagtacatc tacgtattag tcatcgctat taccatggtg atgcggtttt ggcagtacac 540 caatgggcgt ggatagcggt ttgactcacg gggatttcca agtctccacc ccattgacgt 600 caatgggagt ttgttttggc accaaaatca acgggacttt ccaaaatgtc gtaacaactg 660 cgatcgcccg ccccgttgac gcaaatgggc ggtaggcgtg tacggtggga ggtctatata 720 agcagagctc gtttagtgaa ccgtcagatc actagaagct ttattgcggt agtttatcac 780 agttaaattg ctaacgcagt cagtgcttct gacacaacag tctcgaactt aagctgcagt 840 gactctctta aggtagcctt gcagaagttg gtcgtgaggc actgggcagg taagtatcaa 900 ggttacaaga caggtttaag gagaccaata gaaactgggc ttgtcgagac agagaagact 960 cttgcgtttc tgataggcac ctattggtct tactgacatc cactttgcct ttctctccac 1020 aggtgtccac tcccagttca attacagctc ttaaggctag agtacttaat acgactcact 1080 ataggctagg gcccagagca ag atg tgt cac cag cag ttg gtc atc tct tgg 1132 Met Cys His Gln Gln Leu Val Ile Ser Trp 1 5 10 ttt tcc ctg gtt ttt ctg gca tct ccc ctc gtg gcc ata tgg gaa ctg 1180 Phe Ser Leu Val Phe Leu Ala Ser Pro Leu Val Ala Ile Trp Glu Leu 15 20 25 aag aaa gat gtt tat gtc gta gaa ttg gat tgg tat ccg gat gcc cct 1228 Lys Lys Asp Val Tyr Val Val Glu Leu Asp Trp Tyr Pro Asp Ala Pro 30 35 40 gga gaa atg gtg gtc ctc acc tgt gac acc cct gaa gaa gat ggt atc 1276 Gly Glu Met Val Val Leu Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile 45 50 55 acc tgg acc ttg gac cag agc agt gag gtc tta ggc tct ggc aaa acc 1324 Thr Trp Thr Leu Asp Gln Ser Ser Glu Val Leu Gly Ser Gly Lys Thr 60 65 70 ctg acc atc caa gtc aaa gag ttt gga gat gct ggc cag tac acc tgt 1372 Leu Thr Ile Gln Val Lys Glu Phe Gly Asp Ala Gly Gln Tyr Thr Cys 75 80 85 90 cac aaa gga ggc gag gtt cta agc cat tcg ctc ctg ctg ctt cac aaa 1420 His Lys Gly Gly Glu Val Leu Ser His Ser Leu Leu Leu Leu His Lys 95 100 105 aag gaa gat gga att tgg tcc act gat att tta aag gac cag aaa gaa 1468 Lys Glu Asp Gly Ile Trp Ser Thr Asp Ile Leu Lys Asp Gln Lys Glu 110 115 120 ccc aaa aat aag acc ttt cta aga tgc gag gcc aag aat tat tct gga 1516 Pro Lys Asn Lys Thr Phe Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly 125 130 135 cgt ttc acc tgc tgg tgg ctg acg aca atc agt act gat ttg aca ttc 1564 Arg Phe Thr Cys Trp Trp Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe 140 145 150 agt gtc aaa agc agc aga ggc tct tct gac ccc caa ggg gtg acg tgc 1612 Ser Val Lys Ser Ser Arg Gly Ser Ser Asp Pro Gln Gly Val Thr Cys 155 160 165 170 gga gct gct aca ctc tct gca gag aga gtc aga ggg gac aac aag gag 1660 Gly Ala Ala Thr Leu Ser Ala Glu Arg Val Arg Gly Asp Asn Lys Glu 175 180 185 tat gag tac tca gtg gag tgc cag gag gac agt gcc tgc cca gct gct 1708 Tyr Glu Tyr Ser Val Glu Cys Gln Glu Asp Ser Ala Cys Pro Ala Ala 190 195 200 gag gag agt ctg ccc att gag gtc atg gtg gat gcc gtt cac aag ctc 1756 Glu Glu Ser Leu Pro Ile Glu Val Met Val Asp Ala Val His Lys Leu 205 210 215 aag tat gaa aac tac acc agc agc ttc ttc atc agg gac atc atc aaa 1804 Lys Tyr Glu Asn Tyr Thr Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys 220 225 230 cct gac cca ccc aac aac ttg cag ctg aag cca tta aag aat tct cgg 1852 Pro Asp Pro Pro Asn Asn Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg 235 240 245 250 cag gtg gag gtc agc tgg gag tac cct gac acc tgg agt act cca cat 1900 Gln Val Glu Val Ser Trp Glu Tyr Pro Asp Thr Trp Ser Thr Pro His 255 260 265 tcc tac ttc tcc ctg aca ttc tgc gtt cag gtc cag ggc aag agc aag 1948 Ser Tyr Phe Ser Leu Thr Phe Cys Val Gln Val Gln Gly Lys Ser Lys 270 275 280 aga gaa aag aaa gat aga gtc ttc acc gac aag acc tca gcc acg gtc 1996 Arg Glu Lys Lys Asp Arg Val Phe Thr Asp Lys Thr Ser Ala Thr Val 285 290 295 atc tgc cgc aaa aat gcc agc att agc gtg cgg gcc cag gac cgc tac 2044 Ile Cys Arg Lys Asn Ala Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr 300 305 310 tat agc tca tct tgg agc gaa tgg gca tct gtg ccc tgc agt ggt ggc 2092 Tyr Ser Ser Ser Trp Ser Glu Trp Ala Ser Val Pro Cys Ser Gly Gly 315 320 325 330 ggt gga agc ggt ggc ggt gga agc cca tgg aga aac ctc ccc gtg gcc 2140 Gly Gly Ser Gly Gly Gly Gly Ser Pro Trp Arg Asn Leu Pro Val Ala 335 340 345 act cca gac cca gga atg ttc cca tgc ctt cac cac tcc caa aac ctg 2188 Thr Pro Asp Pro Gly Met Phe Pro Cys Leu His His Ser Gln Asn Leu 350 355 360 ctg agg gcc gtc agc aac atg ctc cag aag gcc aga caa act cta gaa 2236 Leu Arg Ala Val Ser Asn Met Leu Gln Lys Ala Arg Gln Thr Leu Glu 365 370 375 ttt tac cct tgc act tct gaa gag att gat cat gaa gat atc aca aaa 2284 Phe Tyr Pro Cys Thr Ser Glu Glu Ile Asp His Glu Asp Ile Thr Lys 380 385 390 gat aaa acc agc aca gtg gag gcc tgt tta cca ttg gaa tta acc aag 2332 Asp Lys Thr Ser Thr Val Glu Ala Cys Leu Pro Leu Glu Leu Thr Lys 395 400 405 410 aat gag agt tgc cta aat tcc aga gag acc tct ttc ata act aat ggg 2380 Asn Glu Ser Cys Leu Asn Ser Arg Glu Thr Ser Phe Ile Thr Asn Gly 415 420 425 agt tgc ctg gcc tcc aga aag acc tct ttt atg atg gcc ctg tgc ctt 2428 Ser Cys Leu Ala Ser Arg Lys Thr Ser Phe Met Met Ala Leu Cys Leu 430 435 440 agt agt att tat gaa gac ttg aag atg tac cag gtg gag ttc aag acc 2476 Ser Ser Ile Tyr Glu Asp Leu Lys Met Tyr Gln Val Glu Phe Lys Thr 445 450 455 atg aat gca aag ctt ctg atg gat cct aag agg cag atc ttt cta gat 2524 Met Asn Ala Lys Leu Leu Met Asp Pro Lys Arg Gln Ile Phe Leu Asp 460 465 470 caa aac atg ctg gca gtt att gat gag ctg atg cag gcc ctg aat ttc 2572 Gln Asn Met Leu Ala Val Ile Asp Glu Leu Met Gln Ala Leu Asn Phe 475 480 485 490 aac agt gag act gtg cca caa aaa tcc tcc ctt gaa gaa ccg gat ttt 2620 Asn Ser Glu Thr Val Pro Gln Lys Ser Ser Leu Glu Glu Pro Asp Phe 495 500 505 tat aaa act aaa atc aag ctc tgc ata ctt ctt cat gct ttc aga att 2668 Tyr Lys Thr Lys Ile Lys Leu Cys Ile Leu Leu His Ala Phe Arg Ile 510 515 520 cgg gca gtg act att gat aga gtg atg agc tat ctg aat gct tcc taa 2716 Arg Ala Val Thr Ile Asp Arg Val Met Ser Tyr Leu Asn Ala Ser 525 530 535 aaagcgaggt acgcgtcgag catgcatcta gggcggccaa ttccgcccct ctccctcccc 2776 cccccctaac gttactggcc gaagccgctt ggaataaggc cggtgtgcgt ttgtctatat 2836 gtgattttcc accatattgc cgtcttttgg caatgtgagg gcccggaaac ctggccctgt 2896 cttcttgacg agcattccta ggggtctttc ccctctcgcc aaaggaatgc aaggtctgtt 2956 gaatgtcgtg aaggaagcag ttcctctgga agcttcttga agacaaacaa cgtctgtagc 3016 gaccctttgc aggcagcgga accccccacc tggcgacagg tgcctctgcg gccaaaagcc 3076 acgtgtataa gatacacctg caaaggcggc acaaccccag tgccacgttg tgagttggat 3136 agttgtggaa agagtcaaat ggctctcctc aagcgtattc aacaaggggc tgaaggatgc 3196 ccagaaggta ccccattgta tgggatctga tctggggcct cggtgcacat gctttacatg 3256 tgtttagtcg aggttaaaaa aacgtctagg ccccccgaac cacggggacg tggttttcct 3316 ttgaaaaaca cgatgataag cttgccacaa cccgggatcc tctagagtcg acatgggcca 3376 cacacggagg cagggaacat caccatccaa gtgtccatac ctcaatttct ttcagctctt 3436 ggtgctggct ggtctttctc acttctgttc aggtgttatc cacgtgacca aggaagtgaa 3496 agaagtggca acgctgtcct gtggtcacaa tgtttctgtt gaagagctgg cacaaactcg 3556 catctactgg caaaaggaga agaaaatggt gctgactatg atgtctgggg acatgaatat 3616 atggcccgag tacaagaacc ggaccatctt tgatatcact aataacctct ccattgtgat 3676 cctggctctg cgcccatctg acgagggcac atacgagtgt gttgttctga agtatgaaaa 3736 agacgctttc aagcgggaac acctggctga agtgacgtta tcagtcaaag ctgacttccc 3796 tacacctagt atatctgact ttgaaattcc aacttctaat attagaagga taatttgctc 3856 aacctctgga ggttttccag agcctcacct ctcctggttg gaaaatggag aagaattaaa 3916 tgccatcaac acaacagttt cccaagatcc tgaaactgag ctctatgctg ttagcagcaa 3976 actggatttc aatatgacaa ccaaccacag cttcatgtgt ctcatcaagt atggacattt 4036 aagagtgaat cagaccttca actggaatac aaccaagcaa gagcattttc ctgataacct 4096 gctcccatcc tgggccatta ccttaatctc agtaaatgga atttttgtga tatgctgcct 4156 gacctactgc tttgccccaa gatgcagaga gagaaggagg aatgagagat tgagaaggga 4216 aagtgtacgc cctgtataac agtgtccgca gaagcaaggg gctgaaacgg ccgatcacta 4276 gtgaattcgc ggccgcttcc ctttagtgag ggttaatgct tcgagcagac atgataagat 4336 acattgatga gtttggacaa accacaacta gaatgcagtg aaaaaaatgc tttatttgtg 4396 aaatttgtga tgctattgct ttatttgtaa ccattataag ctgcaataaa caagttaaca 4456 acaacaattg cattcatttt atgtttcagg ttcaggggga gatgtgggag gttttttaaa 4516 gcaagtaaaa cctctacaaa tgtggtaaaa tccgataagg atcgatccgg gctggcgtaa 4576 tagcgaagag gcccgcaccg atcgcccttc ccaacagttg cgcagcctga atggcgaatg 4636 gacgcgccct gtagcggcgc attaagcgcg gcgggtgtgg tggttacgcg cagcgtgacc 4696 gctacacttg ccagcgccct agcgcccgct cctttcgctt tcttcccttc ctttctcgcc 4756 acgttcgccg gctttccccg tcaagctcta aatcgggggc tccctttagg gttccgattt 4816 agagctttac ggcacctcga ccgcaaaaaa cttgatttgg gtgatggttc acgtagtggg 4876 ccatcgccct gatagacggt ttttcgccct ttgacgttgg agtccacgtt ctttaatagt 4936 ggactcttgt tccaaactgg aacaacactc aaccctatct cggtctattc ttttgattta 4996 taagggattt tgccgatttc ggcctattgg ttaaaaaatg agctgattta acaaatattt 5056 aacgcgaatt ttaacaaaat attaacgttt acaatttcgc ctgatgcggt attttctcct 5116 tacgcatctg tgcggtattt cacaccgcat acgcggatct gcgcagcacc atggcctgaa 5176 ataacctctg aaagaggaac ttggttaggt accttctgag gcggaaagaa ccagctgtgg 5236 aatgtgtgtc agttagggtg tggaaagtcc ccaggctccc cagcaggcag aagtatgcaa 5296 agcatgcatc tcaattagtc agcaaccagg tgtggaaagt ccccaggctc cccagcaggc 5356 agaagtatgc aaagcatgca tctcaattag tcagcaacca tagtcccgcc cctaactccg 5416 cccatcccgc ccctaactcc gcccagttcc gcccattctc cgccccatgg ctgactaatt 5476 ttttttattt atgcagaggc cgaggccgcc tcggcctctg agctattcca gaagtagtga 5536 ggaggctttt ttggaggcct aggcttttgc aaaaagcttg attcttctga cacaacagtc 5596 tcgaacttaa ggctagagcc accatgattg aacaagatgg attgcacgca ggttctccgg 5656 ccgcttgggt ggagaggcta ttcggctatg actgggcaca acagacaatc ggctgctctg 5716 atgccgccgt gttccggctg tcagcgcagg ggcgcccggt tctttttgtc aagaccgacc 5776 tgtccggtgc cctgaatgaa ctgcaggacg aggcagcgcg gctatcgtgg ctggccacga 5836 cgggcgttcc ttgcgcagct gtgctcgacg ttgtcactga agcgggaagg gactggctgc 5896 tattgggcga agtgccgggg caggatctcc tgtcatctca ccttgctcct gccgagaaag 5956 tatccatcat ggctgatgca atgcggcggc tgcatacgct tgatccggct acctgcccat 6016 tcgaccacca agcgaaacat cgcatcgagc gagcacgtac tcggatggaa gccggtcttg 6076 tcgatcagga tgatctggac gaagagcatc aggggctcgc gccagccgaa ctgttcgcca 6136 ggctcaaggc gcgcatgccc gacggcgagg atctcgtcgt gacccatggc gatgcctgct 6196 tgccgaatat catggtggaa aatggccgct tttctggatt catcgactgt ggccggctgg 6256 gtgtggcgga ccgctatcag gacatagcgt tggctacccg tgatattgct gaagagcttg 6316 gcggcgaatg ggctgaccgc ttcctcgtgc tttacggtat cgccgctccc gattcgcagc 6376 gcatcgcctt ctatcgcctt cttgacgagt tcttctgagc gggactctgg ggttcgaaat 6436 gaccgaccaa gcgacgccca acctgccatc acgatggccg caataaaata tctttatttt 6496 cattacatct gtgtgttggt tttttgtgtg aatcgatagc gataaggatc cgcgtatggt 6556 gcactctcag tacaatctgc tctgatgccg catagttaag ccagccccga cacccgccaa 6616 cacccgctga cgcgccctga cgggcttgtc tgctcccggc atccgcttac agacaagctg 6676 tgaccgtctc cgggagctgc atgtgtcaga ggttttcacc gtcatcaccg aaacgcgcga 6736 gacgaaaggg cctcgtgata cgcctatttt tataggttaa tgtcatgata ataatggttt 6796 cttagacgtc aggtggcact tttcggggaa atgtgcgcgg aacccctatt tgtttatttt 6856 tctaaataca ttcaaatatg tatccgctca tgagacaata accctgataa atgcttcaat 6916 aatattgaaa aaggaagagt atgagtattc aacatttccg tgtcgccctt attccctttt 6976 ttgcggcatt ttgccttcct gtttttgctc acccagaaac gctggtgaaa gtaaaagatg 7036 ctgaagatca gttgggtgca cgagtgggtt acatcgaact ggatctcaac agcggtaaga 7096 tccttgagag ttttcgcccc gaagaacgtt ttccaatgat gagcactttt aaagttctgc 7156 tatgtggcgc ggtattatcc cgtattgacg ccgggcaaga gcaactcggt cgccgcatac 7216 actattctca gaatgacttg gttgagtact caccagtcac agaaaagcat cttacggatg 7276 gcatgacagt aagagaatta tgcagtgctg ccataaccat gagtgataac actgcggcca 7336 acttacttct gacaacgatc ggaggaccga aggagctaac cgcttttttg cacaacatgg 7396 gggatcatgt aactcgcctt gatcgttggg aaccggagct gaatgaagcc ataccaaacg 7456 acgagcgtga caccacgatg cctgtagcaa tggcaacaac gttgcgcaaa ctattaactg 7516 gcgaactact tactctagct tcccggcaac aattaataga ctggatggag gcggataaag 7576 ttgcaggacc acttctgcgc tcggcccttc cggctggctg gtttattgct gataaatctg 7636 gagccggtga gcgtgggtct cgcggtatca ttgcagcact ggggccagat ggtaagccct 7696 cccgtatcgt agttatctac acgacgggga gtcaggcaac tatggatgaa cgaaatagac 7756 agatcgctga gataggtgcc tcactgatta agcattggta actgtcagac caagtttact 7816 catatatact ttagattgat ttaaaacttc atttttaatt taaaaggatc taggtgaaga 7876 tcctttttga taatctcatg accaaaatcc cttaacgtga gttttcgttc cactgagcgt 7936 cagaccccgt agaaaagatc aaaggatctt cttgagatcc tttttttctg cgcgtaatct 7996 gctgcttgca aacaaaaaaa ccaccgctac cagcggtggt ttgtttgccg gatcaagagc 8056 taccaactct ttttccgaag gtaactggct tcagcagagc gcagatacca aatactgtcc 8116 ttctagtgta gccgtagtta ggccaccact tcaagaactc tgtagcaccg cctacatacc 8176 tcgctctgct aatcctgtta ccagtggctg ctgccagtgg cgataagtcg tgtcttaccg 8236 ggttggactc aagacgatag ttaccggata aggcgcagcg gtcgggctga acggggggtt 8296 cgtgcacaca gcccagcttg gagcgaacga cctacaccga actgagatac ctacagcgtg 8356 agctatgaga aagcgccacg cttcccgaag ggagaaaggc ggacaggtat ccggtaagcg 8416 gcagggtcgg aacaggagag cgcacgaggg agcttccagg gggaaacgcc tggtatcttt 8476 atagtcctgt cgggtttcgc cacctctgac ttgagcgtcg atttttgtga tgctcgtcag 8536 gggggcggag cctatggaaa aacgccagca acgcggcctt tttacggttc ctggcctttt 8596 gctggccttt tgctcacatg gctcgacaga tct 8629 16 537 PRT Artificial Sequence Description of Artificial Sequence plasmid 16 Met Cys His Gln Gln Leu Val Ile Ser Trp Phe Ser Leu Val Phe Leu 1 5 10 15 Ala Ser Pro Leu Val Ala Ile Trp Glu Leu Lys Lys Asp Val Tyr Val 20 25 30 Val Glu Leu Asp Trp Tyr Pro Asp Ala Pro Gly Glu Met Val Val Leu 35 40 45 Thr Cys Asp Thr Pro Glu Glu Asp Gly Ile Thr Trp Thr Leu Asp Gln 50 55 60 Ser Ser Glu Val Leu Gly Ser Gly Lys Thr Leu Thr Ile Gln Val Lys 65 70 75 80 Glu Phe Gly Asp Ala Gly Gln Tyr Thr Cys His Lys Gly Gly Glu Val 85 90 95 Leu Ser His Ser Leu Leu Leu Leu His Lys Lys Glu Asp Gly Ile Trp 100 105 110 Ser Thr Asp Ile Leu Lys Asp Gln Lys Glu Pro Lys Asn Lys Thr Phe 115 120 125 Leu Arg Cys Glu Ala Lys Asn Tyr Ser Gly Arg Phe Thr Cys Trp Trp 130 135 140 Leu Thr Thr Ile Ser Thr Asp Leu Thr Phe Ser Val Lys Ser Ser Arg 145 150 155 160 Gly Ser Ser Asp Pro Gln Gly Val Thr Cys Gly Ala Ala Thr Leu Ser 165 170 175 Ala Glu Arg Val Arg Gly Asp Asn Lys Glu Tyr Glu Tyr Ser Val Glu 180 185 190 Cys Gln Glu Asp Ser Ala Cys Pro Ala Ala Glu Glu Ser Leu Pro Ile 195 200 205 Glu Val Met Val Asp Ala Val His Lys Leu Lys Tyr Glu Asn Tyr Thr 210 215 220 Ser Ser Phe Phe Ile Arg Asp Ile Ile Lys Pro Asp Pro Pro Asn Asn 225 230 235 240 Leu Gln Leu Lys Pro Leu Lys Asn Ser Arg Gln Val Glu Val Ser Trp 245 250 255 Glu Tyr Pro Asp Thr Trp Ser Thr Pro His Ser Tyr Phe Ser Leu Thr 260 265 270 Phe Cys Val Gln Val Gln Gly Lys Ser Lys Arg Glu Lys Lys Asp Arg 275 280 285 Val Phe Thr Asp Lys Thr Ser Ala Thr Val Ile Cys Arg Lys Asn Ala 290 295 300 Ser Ile Ser Val Arg Ala Gln Asp Arg Tyr Tyr Ser Ser Ser Trp Ser 305 310 315 320 Glu Trp Ala Ser Val Pro Cys Ser Gly Gly Gly Gly Ser Gly Gly Gly 325 330 335 Gly Ser Pro Trp Arg Asn Leu Pro Val Ala Thr Pro Asp Pro Gly Met 340 345 350 Phe Pro Cys Leu His His Ser Gln Asn Leu Leu Arg Ala Val Ser Asn 355 360 365 Met Leu Gln Lys Ala Arg Gln Thr Leu Glu Phe Tyr Pro Cys Thr Ser 370 375 380 Glu Glu Ile Asp His Glu Asp Ile Thr Lys Asp Lys Thr Ser Thr Val 385 390 395 400 Glu Ala Cys Leu Pro Leu Glu Leu Thr Lys Asn Glu Ser Cys Leu Asn 405 410 415 Ser Arg Glu Thr Ser Phe Ile Thr Asn Gly Ser Cys Leu Ala Ser Arg 420 425 430 Lys Thr Ser Phe Met Met Ala Leu Cys Leu Ser Ser Ile Tyr Glu Asp 435 440 445 Leu Lys Met Tyr Gln Val Glu Phe Lys Thr Met Asn Ala Lys Leu Leu 450 455 460 Met Asp Pro Lys Arg Gln Ile Phe Leu Asp Gln Asn Met Leu Ala Val 465 470 475 480 Ile Asp Glu Leu Met Gln Ala Leu Asn Phe Asn Ser Glu Thr Val Pro 485 490 495 Gln Lys Ser Ser Leu Glu Glu Pro Asp Phe Tyr Lys Thr Lys Ile Lys 500 505 510 Leu Cys Ile Leu Leu His Ala Phe Arg Ile Arg Ala Val Thr Ile Asp 515 520 525 Arg Val Met Ser Tyr Leu Asn Ala Ser 530 535 

1. A method of eliciting an anti-tumor immune response in a patient comprising: isolating cancerous cells from a patient; transfecting said cancerous cells with an expression vector system comprising a DNA molecule encoding IL-12 and a costimulatory molecule operably linked to a promoter capable of directing expression of said DNA molecule in said cancerous cells; incubating said transfected cells under conditions whereby the IL-12 and the costimulatory molecules are expressed; and eliciting an anti-tumor immune response in the patient by injecting said transfected cells into the patient.
 2. The method according to claim 1 including irradiating the cancerous cells to prevent replication of the cancerous cells prior to injection of the cancerous cells into the patient.
 3. The method according to claim 1 wherein IL-12 is a single gene fusion of p35 and p40.
 4. The method according to claim 1 wherein the costimulatory molecule is B7-1.
 5. A method of vaccinating an individual comprising: providing cancerous cells isolated from a donor; transfecting said cancerous cells with an expression vector system comprising a DNA molecule encoding IL-12 and a costimulatory molecule operably linked to a promoter capable of directing expression of said DNA molecule in said cancerous cells; incubating said transfected cells under conditions whereby the IL-12 and the costimulatory molecules are expressed; isolating naive T cells from the individual; exposing the T cells to the transfected cancerous cells, thereby activating the T cells; separating the active T cells from the transfected cancerous cells; and injecting the activated T cells into the patient.
 6. The method according to claim 5 wherein IL-12 is a single gene fusion of p35 and p40.
 7. The method according to claim 5 wherein the costimulatory molecule is B7-1.
 8. An expression system comprising a DNA molecule encoding IL-12 and a costimulatory molecule operably linked to a promoter.
 9. The expression system according to claim 8 wherein the IL-12 comprises a fusion of p35 and p40.
 10. The expression system according to claim 8 wherein the costimulatory molecule is selected from the group consisting of: B7-1; B7-2 and CD40L.
 11. The expression system according to claim 8 wherein the costimulatory molecule is B7-1.
 12. A cancerous cell transfected with the expression system of claim
 8. 13. An anti-cancer vaccine comprising the cancerous cell of claim 12 and a suitable excipient. 